NDC 70771-1365 – Nifedipine

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

Human Prescription Drug

Product NDC70771-1365

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Zydus Lifesciences Limited
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 (6)

Package NDCDescriptionSince
70771-1365-01000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-0)Aug 18, 2018
70771-1365-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-1)Aug 18, 2018
70771-1365-410 BLISTER PACK in 1 CARTON (70771-1365-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKAug 18, 2018
70771-1365-5500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-5)Aug 18, 2018
70771-1365-7300 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-7)Aug 18, 2018
70771-1365-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-9)Aug 18, 2018

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