NDC 71335-9651 – Nifedipine

Nifedipine 90 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-9651

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203126
Marketed since
November 1, 2014
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nifedipine →

Package NDC codes (5)

Package NDCDescriptionSince
71335-9651-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9651-1)Feb 21, 2023
71335-9651-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9651-2)Feb 21, 2023
71335-9651-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9651-3)Feb 21, 2023
71335-9651-4180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9651-4)Feb 21, 2023
71335-9651-5100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9651-5)Feb 21, 2023

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