NDC 68084-597 – Nifedipine

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

Human Prescription Drug

Product NDC68084-597

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077127
Marketed since
June 13, 2012
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nifedipine →

Package NDC codes (2)

Package NDCDescriptionSince
68084-597-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-597-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-597-11)Jun 13, 2012
68084-597-6550 BLISTER PACK in 1 CARTON (68084-597-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-597-11)Feb 6, 2023

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