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Prescription medicine

Folic acid Brand names: Quiofic

Folic acid (Quiofic) is a prescription medicine with an FDA approval on record since 1947. FDA's NDC Directory lists it from 29 generic labelers, and pharmacies paid $0.0201 per folic acid 1 mg tablet in the October 7, 2026 NADAC survey.

  • Generic listed

Check it at the source: the folic acid FDA label on DailyMed (effective July 24, 2026, Rising Pharma Holdings, Inc.); the NDA 6135 record on Drugs@FDA; every folic acid label on DailyMed.

Highlights of the record

FDA label of July 24, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026; NADAC October 7, 2026

Used for

From the label: indications and usage

Folic acid, USP is effective in the treatment of megaloblastic anemias due to a deficiency of folic acid, USP (as may be seen in tropical or nontropical sprue) and in anemias of nutritional origin, pregnancy, infancy, or childhood.

Forms and strengths

  • 1 mg
  • 1 mg/5ml
  • 5 mg/ml

Tablet; solution; injection (solution).

On the market

Earliest approval on file
June 2, 1947 Folic Acid, Lilly; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
34 first December 23, 1971; 10 with a marketed status in Drugs@FDA
Labelers listed (NDC)
31 of which 29 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
$0.0201 per tablet Folic acid 1 mg tablet
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
3 since 2012 0 Class I among all firms' recalls; latest January 26, 2022; 25 more by firms not listed as its makers
FAERS reports
247,883 through July 30, 2026

What is folic acid used for?

From the label: indications and usage

Folic acid, USP is effective in the treatment of megaloblastic anemias due to a deficiency of folic acid, USP (as may be seen in tropical or nontropical sprue) and in anemias of nutritional origin, pregnancy, infancy, or childhood.

Source: FDA drug label (Folic Acid), Rising Pharma Holdings, Inc., effective July 24, 2026 (SPL set 0baa10dd-6d1d-4946-8236-566451132da3), via openFDA; the full label on DailyMed

Is there a generic for folic acid (Quiofic)?

The FDA approved the first generic folic acid on December 23, 1971. 34 generic applications are approved; 10 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 folic acid from 29 labelers under a generic (ANDA) application and from 1 brand labeler. A listing means the company has registered the product for sale; it does not show that every pharmacy stocks it.

  • 1947 earliest approval on file
  • 1971 first generic approved
  • red ticks recalls

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

What do pharmacies pay for folic acid (Quiofic)?

In CMS's NADAC survey of October 7, 2026, pharmacies paid $0.0201 per Folic acid 1 mg tablet, down 11% from $0.0226 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.

  • Folic acid 1 mg tablet (generic)
$0.0288
$0.0173
January 2024October 2026
NADAC per unit, October 7, 2026
Strength and formBrand or genericPharmacy cost30 tablets, or one pen or vial12-month change
Folic acid 1 mg tabletGeneric$0.0201 per tablet$0.604-11%

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

Has folic acid been recalled?

The FDA's Enforcement Report lists 28 recalls naming folic acid since 2012: 0 Class I (the most serious), 26 Class II, 2 Class III; 1 still ongoing. 25 of them are by firms that FDA's NDC Directory does not list as a maker of folic acid 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
May 9, 2022Class IIOlympia Compounding Pharmacy dba Olympia Pharmacy not a listed makerLack of assurance of sterility.
March 7, 2022Class IITMC Acquisition LLC dba Tailor Made Compounding not a listed makerLack of Assurance of Sterility
January 26, 2022Class IICARDINAL HEALTHCARECGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
August 13, 2021Class IIFirst Royal Care Co. LLC, dba Red Mountain Compounding … not a listed makerLack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
June 19, 2019Class IIRXQ Compounding LLC not a listed makerLack of Assurance of Sterility
December 17, 2018Class IIPromise Pharmacy, LLC not a listed makerLack of sterility assurance.
August 21, 2018Class IIAuro Pharmacies, Inc. not a listed makerLack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
April 18, 2017Class IIKey Pharmacy and Compounding Center not a listed makerLack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

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

What does the folic acid label say about other medicines?

The folic acid label names 16 other medicines 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
Carbamazepinedrug interactionsEnzyme-inducing anticonvulsants such as phenytoin, primidone, carbamazepine, phenobarbital, and the broader anticonvulsant class increase hepatic folate metabolism, inhibit intestinal folate-processing enzymes, raise gastrointestinal pH, or displace folate from serum proteins, collectively leading to decreased folate …
Cholestyraminedrug interactionsAdditional agents such as pentamidine, antacids, cholestyramine, colestipol, and H 2 blockers impair gastrointestinal folate uptake through pH elevation, transporter inhibition, or binding of dietary folate.
Colestipoldrug interactionsAdditional agents such as pentamidine, antacids, cholestyramine, colestipol, and H 2 blockers impair gastrointestinal folate uptake through pH elevation, transporter inhibition, or binding of dietary folate.
Cycloserinedrug interactionsValproate and sulfasalazine primarily reduce intestinal folate absorption or interfere with folate-dependent metabolic pathways, while isoniazid and cycloserine reduce folate utilization through metabolic disruption.
Isoniaziddrug interactionsValproate and sulfasalazine primarily reduce intestinal folate absorption or interfere with folate-dependent metabolic pathways, while isoniazid and cycloserine reduce folate utilization through metabolic disruption.
Methotrexatedrug interactionsFolate deficiency may result from increased loss of folate, as in renal dialysis and/or interference with metabolism (e.g., folic acid antagonists such as methotrexate); the administration of anticonvulsants, such as diphenylhydantoin, primidone, and barbiturates; …
Nitrofurantoindrug interactions… barbiturates; alcohol consumption and, especially, alcoholic cirrhosis; and the administration of pyrimethamine and nitrofurantoin.
Nitrous oxidedrug interactionsNitrous oxide indirectly decreases folate activity by inactivating vitamin B12 and downstream methylation pathways, while oral contraceptives increase folate turnover and urinary loss.
Phenobarbitaldrug interactionsEnzyme-inducing anticonvulsants such as phenytoin, primidone, carbamazepine, phenobarbital, and the broader anticonvulsant class increase hepatic folate metabolism, inhibit intestinal folate-processing enzymes, raise gastrointestinal pH, or displace folate from serum proteins, collectively leading to decreased folate …
Phenytoindrug interactionsA patient whose epilepsy is completely controlled by phenytoin may require increased doses to prevent convulsions if folic acid is given.
Primidonedrug interactionsFolate deficiency may result from increased loss of folate, as in renal dialysis and/or interference with metabolism (e.g., folic acid antagonists such as methotrexate); the administration of anticonvulsants, such as diphenylhydantoin, primidone, and barbiturates; …
Pyrimethaminedrug interactions… primidone, and barbiturates; alcohol consumption and, especially, alcoholic cirrhosis; and the administration of pyrimethamine and nitrofurantoin.
Sulfasalazinedrug interactionsValproate and sulfasalazine primarily reduce intestinal folate absorption or interfere with folate-dependent metabolic pathways, while isoniazid and cycloserine reduce folate utilization through metabolic disruption.
Tetracyclinedrug interactionsFalse low serum and red cell folate levels may occur if the patient has been taking antibiotics, such as tetracycline, which suppress the growth of Lactobacillus casei.

Every other medicine the folic acid label names

Medicine namedSectionWhat the label says
Triamterenedrug interactionsSeveral antifolate agents, including trimethoprim, pyrimethamine, methotrexate, and triamterene, directly inhibit dihydrofolate reductase, decreasing the formation of active folate derivatives.
Trimethoprimdrug interactionsSeveral antifolate agents, including trimethoprim, pyrimethamine, methotrexate, and triamterene, directly inhibit dihydrofolate reductase, decreasing the formation of active folate derivatives.

Check folic acid against other medicines

Source: FDA drug label (Folic Acid), Rising Pharma Holdings, Inc., effective July 24, 2026 (SPL set 0baa10dd-6d1d-4946-8236-566451132da3), via openFDA; the full label on DailyMed

What do FAERS reports show for folic acid?

The FDA Adverse Event Reporting System holds 247,883 reports that list folic acid among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 23,149 are coded as a death and 89,888 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)25,264
  • Fatigue23,921
  • Pain23,620
  • Arthralgia19,991
  • Off Label Use (a use or a product term, not a reaction)18,071
  • Rheumatoid Arthritis17,937
  • Nausea (named in the label)16,045
  • Diarrhoea14,600

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?

Folic acid side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other