NDC 50742-262 – Nifedipine

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

Human Prescription Drug

Product NDC50742-262

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
50742-262-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-262-01)Mar 12, 2019
50742-262-03300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-262-03)Mar 12, 2019
50742-262-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-262-30)Mar 12, 2019

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