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
70752-231_067af2c9-3769-40d4-a991-217390ece384
Product NDC
70752-231
Form
TABLET
Composition / generic term
Folic Acid
Labeler
QUAGEN PHARMACEUTICALS LLC
Marketing category
ANDA
Marketing start / end (source format)
20230710
Source listing expiry
20271231

Source-listed ingredients

  • FOLIC ACID — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (70752-231-10) · 70752-231-10
  • 1000 TABLET in 1 BOTTLE (70752-231-11) · 70752-231-11

Source and coverage

Open FDA National Drug Code directory

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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