NDC 50742-261 – Nifedipine

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

Human Prescription Drug

Product NDC50742-261

Product details

Brand name
Nifedipine
Generic name
nifedipine
Labeler
Ingenus Pharmaceuticals, LLC
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 (3)

Package NDCDescriptionSince
50742-261-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-261-01)Mar 12, 2019
50742-261-03300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-261-03)Mar 12, 2019
50742-261-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-261-30)Mar 12, 2019

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