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
- 71205-965_ba67d6b0-f638-4264-9bd4-1557223abe83
- Product NDC
- 71205-965
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Nifedipine
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141101
- Source listing expiry
- 20261231
Source-listed ingredients
- NIFEDIPINE — 90 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-00) · 71205-965-00
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-30) · 71205-965-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-60) · 71205-965-60
- 240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-64) · 71205-965-64
- 270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-67) · 71205-965-67
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-72) · 71205-965-72
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-78) · 71205-965-78
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-90) · 71205-965-90
- 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-96) · 71205-965-96
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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