NDC 68682-105 – Nifedipine

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

Human Prescription Drug

Product NDC68682-105

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Oceanside Pharmaceuticals
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075269
Marketed since
October 18, 2012
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
68682-105-10100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-10)Oct 18, 2012
68682-105-30300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-30)Oct 18, 2012

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