NDC 62175-262 – Nifedipine

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

Human Prescription Drug

Product NDC62175-262

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Lannett Company, Inc.
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 (3)

Package NDCDescriptionSince
62175-262-3230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-32)Oct 3, 2007
62175-262-37100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-37)Oct 3, 2007
62175-262-4690 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-46)Oct 3, 2007

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