NDC 71335-1721 – Nifedipine

Nifedipine 60 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-1721

Product details

Brand name
Nifedipine
Generic name
nifedipine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210614
Marketed since
March 12, 2019
Listing expires
December 31, 2027
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for nifedipine →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1721-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-1)Oct 20, 2020
71335-1721-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-2)Oct 20, 2020
71335-1721-360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-3)Oct 20, 2020
71335-1721-428 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-4)Oct 20, 2020
71335-1721-510 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-5)Oct 20, 2020

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