United States · FDA National Drug Code directory

Nifedipine

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 50742-620_182d5c87-db57-4042-a1e8-d2c78b07789b
Product NDC: 50742-620
Form: TABLET, EXTENDED RELEASE
Composition / generic term: nifedipine
Labeler: Ingenus Pharmaceuticals, LLC
Marketing category: ANDA
Marketing start / end (source format): 20170215
Source listing expiry: 20271231

Source-listed ingredients

NIFEDIPINE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-620-01) · 50742-620-01

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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