United States · FDA National Drug Code directory
Nimodipine
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
- 69452-209_452704d5-dbeb-5833-e063-6394a90a1a9a
- Product NDC
- 69452-209
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Nimodipine
- Labeler
- BIONPHARMA INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171121
- Source listing expiry
- 20261231
Source-listed ingredients
- NIMODIPINE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (69452-209-13) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK · 69452-209-13
- 10 BLISTER PACK in 1 CARTON (69452-209-20) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK · 69452-209-20
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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