NDC 0904-7082 – Nifedipine

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

Human Prescription Drug 1 recall

Product NDC0904-7082

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Major Pharmaceuticals
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 (2)

Package NDCDescriptionSince
0904-7082-0430 BLISTER PACK in 1 CARTON (0904-7082-04) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMar 12, 2019
0904-7082-0650 BLISTER PACK in 1 CARTON (0904-7082-06) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMar 12, 2019

Recalls mentioning this NDC

Other Nifedipine products