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
- 68682-105_ed2ab44d-7e6a-4c65-8bb0-9d3a4d9bf618
- Product NDC
- 68682-105
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Nifedipine
- Labeler
- Oceanside Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121018
- 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 (68682-105-10) · 68682-105-10
- 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-30) · 68682-105-30
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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