NDC 68382-690 – Nifedipine

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

Human Prescription Drug

Product NDC68382-690

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210184
Marketed since
August 18, 2018
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nifedipine →

Package NDC codes (5)

Package NDCDescriptionSince
68382-690-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-01)Aug 18, 2018
68382-690-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-10)Aug 18, 2018
68382-690-1690 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-16)Aug 18, 2018
68382-690-7710 BLISTER PACK in 1 CARTON (68382-690-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKAug 18, 2018
68382-690-95300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-95)Aug 18, 2018

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