NDC 70807-503 – Nifedipine

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

Human Prescription Drug

Product NDC70807-503

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Elite Pharmaceutical Solution, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212016
Marketed since
October 15, 2021
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
70807-503-12100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-12)Oct 15, 2021
70807-503-13300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-13)Oct 15, 2021

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