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
- 68682-106_2c9ac184-8e21-479c-a1e8-4abeadfb54a1
- Product NDC
- 68682-106
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Nifedipine
- Labeler
- Oceanside Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20001204
- Source listing expiry
- 20271231
Source-listed ingredients
- NIFEDIPINE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-106-10) · 68682-106-10
- 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-106-30) · 68682-106-30
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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