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
11534-165_5250e701-9f7a-42a8-bae9-95c4779f06aa
Product NDC
11534-165
Form
TABLET
Composition / generic term
folic acid
Labeler
SUNRISE PHARMACEUTICAL, INC.
Marketing category
ANDA
Marketing start / end (source format)
20150804
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 (11534-165-01) · 11534-165-01
  • 1000 TABLET in 1 BOTTLE (11534-165-03) · 11534-165-03
  • 90 TABLET in 1 BOTTLE (11534-165-90) · 11534-165-90

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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