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
- 71335-0744_71897d78-4819-40bc-ae39-f735fa929a20
- Product NDC
- 71335-0744
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- nifedipine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20000927
- Source listing expiry
- 20271231
Source-listed ingredients
- NIFEDIPINE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-1) · 71335-0744-1
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-2) · 71335-0744-2
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-3) · 71335-0744-3
- 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-4) · 71335-0744-4
- 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0744-5) · 71335-0744-5
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →