NDC 71335-0766 – Folic Acid

Folic Acid 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0766

Product details

Brand name
Folic Acid
Generic name
Folic Acid
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040796
Marketed since
January 12, 2009
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-0766-130 TABLET in 1 BOTTLE (71335-0766-1)Apr 10, 2018
71335-0766-2100 TABLET in 1 BOTTLE (71335-0766-2)Apr 10, 2018
71335-0766-3120 TABLET in 1 BOTTLE (71335-0766-3)Apr 10, 2018
71335-0766-450 TABLET in 1 BOTTLE (71335-0766-4)Apr 10, 2018
71335-0766-590 TABLET in 1 BOTTLE (71335-0766-5)Apr 10, 2018
71335-0766-660 TABLET in 1 BOTTLE (71335-0766-6)Apr 10, 2018
71335-0766-710 TABLET in 1 BOTTLE (71335-0766-7)Apr 10, 2018

Other Folic Acid products