NDC 68788-8164 – Nifedipine

Nifedipine 60 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC68788-8164

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210614
Marketed since
April 4, 2022
Listing expires
December 31, 2027
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nifedipine →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8164-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8164-1)Apr 4, 2022
68788-8164-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8164-3)Apr 4, 2022
68788-8164-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8164-6)Apr 4, 2022
68788-8164-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8164-9)Apr 4, 2022

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