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
- 71205-913_b78a6505-03e7-4f18-89ef-737f807df7c2
- Product NDC
- 71205-913
- Form
- TABLET
- Composition / generic term
- FOLIC ACID
- Labeler
- Proficient Rx LP
- 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
- 100 TABLET in 1 BOTTLE (71205-913-00) · 71205-913-00
- 1000 TABLET in 1 BOTTLE (71205-913-11) · 71205-913-11
- 30 TABLET in 1 BOTTLE (71205-913-30) · 71205-913-30
- 500 TABLET in 1 BOTTLE (71205-913-55) · 71205-913-55
- 60 TABLET in 1 BOTTLE (71205-913-60) · 71205-913-60
- 90 TABLET in 1 BOTTLE (71205-913-90) · 71205-913-90
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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