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Prescription medicine

Rifampin First approved as Rifadin

Rifampin (Rifadin) is a prescription medicine with an FDA approval on record since 1971. FDA's NDC Directory lists it from 13 generic labelers, and pharmacies paid $0.679 per rifampin 300 mg capsule in the October 7, 2026 NADAC survey.

  • Generic listed
  • In shortage

Check it at the source: the rifampin FDA label on DailyMed (effective February 11, 2026, Lupin Pharmaceuticals, Inc.); the NDA 50420 record on Drugs@FDA; every rifampin label on DailyMed.

Highlights of the record

FDA label of February 11, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026; NADAC October 7, 2026

Used for

From the label: indications and usage

In the treatment of both tuberculosis and the meningococcal carrier state, the small number of resistant cells present within large populations of susceptible cells can rapidly become the predominant type.

Forms and strengths

  • 150 mg
  • 300 mg
  • 600 mg
  • 600 mg/10ml

Capsule; injection (powder) (lyophilized) for solution.

On the market

Earliest approval on file
May 21, 1971 Rifadin, Sanofi Aventis Us; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
12 first May 28, 1997; 9 with a marketed status in Drugs@FDA
Labelers listed (NDC)
13 of which 13 under generic applications, 0 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
$0.679 per capsule Rifampin 300 mg capsule
Shortage (FDA)
7 of 13 presentations limited or unavailable updated October 6, 2026
Recalls by its makers (FDA)
14 since 2014 0 Class I among all firms' recalls; latest March 21, 2024; 7 more by firms not listed as its makers
FAERS reports
14,511 through July 30, 2026

What is rifampin used for?

From the label: indications and usage

In the treatment of both tuberculosis and the meningococcal carrier state, the small number of resistant cells present within large populations of susceptible cells can rapidly become the predominant type. Bacteriologic cultures should be obtained before the start of therapy to confirm the susceptibility of the organism to rifampin and they should be repeated throughout therapy to monitor the response to treatment. Since resistance can emerge rapidly, susceptibility tests should be performed in the event of persistent positive cultures during the course of treatment. If test results show resistance to rifampin and the patient is not responding to therapy, the drug regimen should be modified. […]

FDA pharmacologic class: Rifamycin Antibacterial.

Source: FDA drug label (rifampin), Lupin Pharmaceuticals, Inc., effective February 11, 2026 (SPL set b56004f0-f23d-47f6-80c7-39884fccbccc), via openFDA; the full label on DailyMed

Is there a generic for rifampin (Rifadin)?

The FDA approved the first generic rifampin on May 28, 1997. 12 generic applications are approved; 9 of them carry a current (not discontinued) marketing status in Drugs@FDA; that status is not evidence that the generic is on sale.

FDA's NDC Directory lists rifampin from 13 labelers under a generic (ANDA) application. A listing means the company has registered the product for sale; it does not show that every pharmacy stocks it.

  • 1971 earliest approval on file
  • 1997 first generic approved
  • 2021 to now in shortage
  • red ticks recalls

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What do pharmacies pay for rifampin (Rifadin)?

In CMS's NADAC survey of October 7, 2026, pharmacies paid $0.679 per Rifampin 300 mg capsule, down 4% from $0.704 on October 8, 2025. The chart's scale runs from the lowest to the highest price shown, not from zero. NADAC is what retail pharmacies paid their wholesalers, per unit, in CMS's monthly survey; what a patient pays depends on insurance and the pharmacy.

  • Rifampin 300 mg capsule (generic)
$0.734
$0.489
January 2024October 2026
NADAC per unit, October 7, 2026
Strength and formBrand or genericPharmacy cost30 tablets, or one pen or vial12-month change
Rifampin 150 mg capsuleGeneric$0.898 per capsule$26.93+42%
Rifampin 300 mg capsuleGeneric$0.679 per capsule$20.37-4%

Source: CMS National Average Drug Acquisition Cost (NADAC) survey, October 7, 2026: what retail pharmacies paid per unit; not a counter price

Is rifampin in shortage?

The FDA Drug Shortage Database lists 7 of 13 rifampin presentations as limited or unavailable (updated October 6, 2026); the first entry was posted on February 17, 2021. 5 more presentations are on the list as available.

PresentationCompanyStatusUpdated
Rifadin, Injection, 600 mg (NDC 0068-0597-01)Sanofi-Aventis U.S. LLCCurrentSeptember 18, 2026
Rifampin, Capsule, 150 mg (NDC 42806-801-01)Epic Pharma, LLCCurrentOctober 5, 2026
Rifampin, Capsule, 150 mg (NDC 42806-801-30)Epic Pharma, LLCCurrentOctober 5, 2026
Rifampin, Capsule, 150 mg (NDC 68180-658-06)Lupin Pharmaceuticals, Inc.CurrentSeptember 1, 2026
Rifampin, Capsule, 300 mg (NDC 42806-799-01)Epic Pharma, LLCCurrentOctober 5, 2026
Rifampin, Capsule, 300 mg (NDC 42806-799-05)Epic Pharma, LLCCurrentOctober 5, 2026
Rifampin, Capsule, 300 mg (NDC 42806-799-30)Epic Pharma, LLCCurrentOctober 5, 2026
Rifampin, Capsule, 300 mg (NDC 42806-799-60)Epic Pharma, LLCCurrentOctober 5, 2026

Every rifampin presentation in the FDA shortage database

Source: FDA Drug Shortage Database via openFDA, updated October 8, 2026

Has rifampin been recalled?

The FDA's Enforcement Report lists 21 recalls naming rifampin since 2014: 0 Class I (the most serious), 19 Class II, 2 Class III; 4 still ongoing. 7 of them are by firms that FDA's NDC Directory does not list as a maker of rifampin and that hold no application for it in Drugs@FDA, such as compounding pharmacies or bulk-ingredient suppliers; the recall notice names the product recalled. A recall names products and lots, not every product of the medicine.

StartedClassCompanyReason
March 21, 2024Class IILupin Pharmaceuticals Inc.Subpotent Drug
January 11, 2024Class IIAmerisource Health Services LLCFailed Impurities/Degradation Specification.
January 5, 2024Class IILupin Pharmaceuticals Inc.Subpotent Drug and Failed Impurities/Degradation Specifications
April 26, 2023Class IIAkorn, Inc. not a listed makerCGMP Deviations: Firm went out of business and could no longer continue stability studies.
December 20, 2022Class IIRemedyRepack Inc.Failed Impurities/Degradation specifications
December 20, 2022Class IIAmerisource Health Services LLCFailed Impurities/Degradations Specifications
December 12, 2022Class IILupin Pharmaceuticals Inc.Failed Impurities/Degradation Specifications: Failure observed in related substance testing during long term stability study.
October 6, 2022Class IIGolden State Medical Supply Inc.Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).

Source: FDA Enforcement Report (drug recalls) via openFDA, through October 8, 2026

What does the rifampin label say about other medicines?

The rifampin label names 9 other medicines in its interaction, contraindication or warning sections. The labels of 36 other medicines name rifampin. The sentences are the labels' own; a label lists what its studies and reports found, not every interaction.

Medicine namedSectionWhat the label says
AtazanavircontraindicationsRifampin is contraindicated in patients who are also receiving atazanavir, darunavir, fosamprenavir, saquinavir, tipranavir, cabotegravir, fostemsavir and lenacapavir (see prescribing information for SUNLENCA) due to the potential of rifampin to substantially decrease plasma concentrations of these antiviral drugs …
CabotegravircontraindicationsRifampin is contraindicated in patients who are also receiving atazanavir, darunavir, fosamprenavir, saquinavir, tipranavir, cabotegravir, fostemsavir and lenacapavir (see prescribing information for SUNLENCA) due to the potential of rifampin to substantially decrease plasma concentrations of these antiviral drugs …
CefazolinwarningsPostmarketing reports suggest that concomitant administration of high doses of cefazolin and rifampin may prolong the prothrombin time, leading to severe vitamin K–dependent coagulation disorders that may be life-threatening or fatal.
DarunavircontraindicationsRifampin is contraindicated in patients who are also receiving atazanavir, darunavir, fosamprenavir, saquinavir, tipranavir, cabotegravir, fostemsavir and lenacapavir (see prescribing information for SUNLENCA) due to the potential of rifampin to substantially decrease plasma concentrations of these antiviral drugs …
FosamprenavircontraindicationsRifampin is contraindicated in patients who are also receiving atazanavir, darunavir, fosamprenavir, saquinavir, tipranavir, cabotegravir, fostemsavir and lenacapavir (see prescribing information for SUNLENCA) due to the potential of rifampin to substantially decrease plasma concentrations of these antiviral drugs …
FostemsavircontraindicationsRifampin is contraindicated in patients who are also receiving atazanavir, darunavir, fosamprenavir, saquinavir, tipranavir, cabotegravir, fostemsavir and lenacapavir (see prescribing information for SUNLENCA) due to the potential of rifampin to substantially decrease plasma concentrations of these antiviral drugs …
LenacapavircontraindicationsRifampin is contraindicated in patients who are also receiving atazanavir, darunavir, fosamprenavir, saquinavir, tipranavir, cabotegravir, fostemsavir and lenacapavir (see prescribing information for SUNLENCA) due to the potential of rifampin to substantially decrease plasma concentrations of these antiviral drugs …
LurasidonecontraindicationsRifampin is contraindicated in patients receiving lurasidone.
PraziquantelcontraindicationsRifampin is contraindicated in patients receiving praziquantel since therapeutically effective blood levels of praziquantel may not be achieved.

Other labels that name rifampin

Check rifampin against other medicines

Source: FDA drug label (rifampin), Lupin Pharmaceuticals, Inc., effective February 11, 2026 (SPL set b56004f0-f23d-47f6-80c7-39884fccbccc), via openFDA; the full label on DailyMed

What do FAERS reports show for rifampin?

The FDA Adverse Event Reporting System holds 14,511 reports that list rifampin among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 1,483 are coded as a death and 5,858 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.

Reports received each year

The most reported reactions

  • Drug Ineffective (a use or a product term, not a reaction)1,608
  • Off Label Use (a use or a product term, not a reaction)1,216
  • Drug Interaction (a use or a product term, not a reaction)1,084
  • Drug Reaction With Eosinophilia And Systemic Symptoms (named in the label)746
  • Nausea (named in the label)680
  • Condition Aggravated (a use or a product term, not a reaction)619
  • Product Use In Unapproved Indication (a use or a product term, not a reaction)594
  • Pyrexia571

Side effects: the label's list and every FAERS reaction

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Other rifamycin antibacterials
the pharmacologic class, with prices and generics
Rifampin side effects
the label's list beside FAERS reports
Rifampin shortage record
every presentation, company and date
Check an interaction
what two or more labels say about each other