NDC 46708-732 – Nifedipine

Nifedipine 30 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC46708-732

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216896
Marketed since
November 23, 2022
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
46708-732-31100 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-732-31)Nov 23, 2022
46708-732-63300 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-732-63)Nov 23, 2022
46708-732-911000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-732-91)Nov 23, 2022

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