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
- 68382-687_c0025ef1-99d7-4b31-9d99-4be010b2b9fb
- Product NDC
- 68382-687
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Nifedipine
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180202
- 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 (68382-687-01) · 68382-687-01
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-687-10) · 68382-687-10
- 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-687-95) · 68382-687-95
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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