Skip to main content

Prescription medicine

Eravacycline Brand names: Xerava

Eravacycline (Xerava) is a prescription medicine with an FDA approval on record since 2018. No generic is listed in FDA's NDC Directory.

  • No generic listed

Check it at the source: the eravacycline FDA label on DailyMed (effective March 31, 2025, Tetraphase Pharmaceuticals, Inc.); the NDA 211109 record on Drugs@FDA; every eravacycline label on DailyMed.

Highlights of the record

FDA label of March 31, 2025; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026

Used for

From the label: indications and usage

XERAVA is a tetracycline class antibacterial indicated for the treatment of complicated intra‑abdominal infections in patients 18 years of age and older.

Forms and strengths

  • 50 mg
  • 100 mg

Injection (powder) (lyophilized) for solution.

On the market

Earliest approval on file
August 27, 2018 Xerava, Tetraphase Pharms; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
No generic approved
Labelers listed (NDC)
1 of which 0 under generic applications, 1 under brand applications, repackagers included
Last listed patent
October 19, 2037 Xerava injection; not a generic launch date

Supply and safety

Pharmacy cost (NADAC)
Not in the survey
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
243 through July 30, 2026

What is eravacycline used for?

From the label: indications and usage

XERAVA is a tetracycline class antibacterial indicated for the treatment of complicated intra‑abdominal infections in patients 18 years of age and older. ( 1.1 ) Limitations of Use XERAVA is not indicated for the treatment of complicated urinary tract infections (cUTI). ( 1.1 ) To reduce the development of drug-resistant bacteria and maintain the effectiveness of XERAVA and other antibacterial drugs, XERAVA should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. […]

FDA pharmacologic class: Tetracycline-class Antibacterial.

Source: FDA drug label (Xerava), Tetraphase Pharmaceuticals, Inc., effective March 31, 2025 (SPL set a4b188d4-f467-470c-ad7b-25ffbdd8862a), via openFDA; the full label on DailyMed

Is there a generic for eravacycline (Xerava)?

No generic eravacycline is approved (Drugs@FDA, October 8, 2026).

The Orange Book lists 4 patents for Xerava injection: the compound patent runs to October 19, 2037. A patent or exclusivity date is not the date a generic goes on sale: court cases and settlements move it either way.

  • 2018 earliest approval on file
  • 2037 last listed patent

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

What does the eravacycline label say about other medicines?

The eravacycline label names 1 other medicine in its interaction, contraindication or warning sections. The sentences are the labels' own; a label lists what its studies and reports found, not every interaction.

Medicine namedSectionWhat the label says
Tetracyclinewarnings and precautionsA decrease in fibula growth rate has been observed in premature infants given oral tetracycline in doses of 25 mg/kg every 6 hours.

Check eravacycline against other medicines

Source: FDA drug label (Xerava), Tetraphase Pharmaceuticals, Inc., effective March 31, 2025 (SPL set a4b188d4-f467-470c-ad7b-25ffbdd8862a), via openFDA; the full label on DailyMed

What do FAERS reports show for eravacycline?

The FDA Adverse Event Reporting System holds 243 reports that list eravacycline among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 43 are coded as a death and 68 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.

The most reported reactions

  • Off Label Use (a use or a product term, not a reaction)73
  • Drug Ineffective (a use or a product term, not a reaction)30
  • Blood Fibrinogen Decreased17
  • Nausea (named in the label)16
  • Thrombocytopenia15
  • Multiple Organ Dysfunction Syndrome14
  • Product Use In Unapproved Indication (a use or a product term, not a reaction)14
  • Diarrhoea (named in the label)12

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 tetracycline-class antibacterials
the pharmacologic class, with prices and generics
Eravacycline side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other