NDC 68682-108 – Nifedipine

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

Human Prescription Drug

Product NDC68682-108

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Oceanside Pharmaceuticals
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075289
Marketed since
September 27, 2000
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
68682-108-10100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-10)Sep 27, 2000
68682-108-30300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-30)Sep 27, 2000

Other Nifedipine products