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
62135-210_2589605c-12b7-ed10-e063-6294a90ab52b
Product NDC
62135-210
Form
TABLET
Composition / generic term
Folic Acid
Labeler
Chartwell RX, LLC.
Marketing category
ANDA
Marketing start / end (source format)
20190530
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 (62135-210-01) · 62135-210-01
  • 500 TABLET in 1 BOTTLE (62135-210-05) · 62135-210-05
  • 1000 TABLET in 1 BOTTLE (62135-210-10) · 62135-210-10
  • 1800 TABLET in 1 BOTTLE (62135-210-72) · 62135-210-72
  • 90 TABLET in 1 BOTTLE (62135-210-90) · 62135-210-90
  • 3000 TABLET in 1 BOTTLE (62135-210-97) · 62135-210-97

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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