NDC 71335-0613 – Folic Acid

Folic Acid 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0613

Product details

Brand name
Folic Acid
Generic name
Folic acid
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204418
Marketed since
August 4, 2015
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Folic Acid →

Package NDC codes (7)

Package NDCDescriptionSince
71335-0613-130 TABLET in 1 BOTTLE (71335-0613-1)Jul 14, 2021
71335-0613-2100 TABLET in 1 BOTTLE (71335-0613-2)Jun 9, 2021
71335-0613-3120 TABLET in 1 BOTTLE (71335-0613-3)Jan 28, 2025
71335-0613-450 TABLET in 1 BOTTLE (71335-0613-4)Jan 28, 2025
71335-0613-590 TABLET in 1 BOTTLE (71335-0613-5)Jan 28, 2025
71335-0613-660 TABLET in 1 BOTTLE (71335-0613-6)Jan 28, 2025
71335-0613-710 TABLET in 1 BOTTLE (71335-0613-7)Jan 28, 2025

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