United States · FDA National Drug Code directory
FOLIC ACID
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71335-0766_291dfcdf-7bc5-4313-a533-25c72defdd72
- Product NDC
- 71335-0766
- Form
- TABLET
- Composition / generic term
- FOLIC ACID
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090112
- Source listing expiry
- 20261231
Source-listed ingredients
- FOLIC ACID — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-0766-1) · 71335-0766-1
- 100 TABLET in 1 BOTTLE (71335-0766-2) · 71335-0766-2
- 120 TABLET in 1 BOTTLE (71335-0766-3) · 71335-0766-3
- 50 TABLET in 1 BOTTLE (71335-0766-4) · 71335-0766-4
- 90 TABLET in 1 BOTTLE (71335-0766-5) · 71335-0766-5
- 60 TABLET in 1 BOTTLE (71335-0766-6) · 71335-0766-6
- 10 TABLET in 1 BOTTLE (71335-0766-7) · 71335-0766-7
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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