NDC 71335-0744 – Nifedipine

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

Human Prescription Drug

Product NDC71335-0744

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075289
Marketed since
September 27, 2000
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
71335-0744-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-1)Mar 21, 2018
71335-0744-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-2)Mar 21, 2018
71335-0744-360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-3)Mar 21, 2018
71335-0744-428 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-4)Mar 21, 2018
71335-0744-510 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-5)Mar 21, 2018

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