NDC 71205-963 – Nifedipine

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

Human Prescription Drug

Product NDC71205-963

Product details

Brand name
Nifedipine
Generic name
Nifedipine
Labeler
Proficient Rx LP
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203126
Marketed since
November 1, 2014
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nifedipine →

Package NDC codes (9)

Package NDCDescriptionSince
71205-963-00100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-00)Jun 9, 2020
71205-963-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-30)Oct 6, 2020
71205-963-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-60)Oct 6, 2020
71205-963-64240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-64)Oct 6, 2020
71205-963-67270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-67)Oct 6, 2020
71205-963-72120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-72)Oct 6, 2020
71205-963-78180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-78)Oct 6, 2020
71205-963-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-90)Oct 6, 2020
71205-963-96300 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-96)Jun 9, 2020

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