NDC 62135-523 – Nifedipine

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

Human Prescription Drug

Product NDC62135-523

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Chartwell RX, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077127
Marketed since
October 3, 2007
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nifedipine →

Package NDC codes (1)

Package NDCDescriptionSince
62135-523-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-523-90)Apr 11, 2023

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