United States · FDA National Drug Code directory
Miconazole Nitrate
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
- 0472-1738_bb1aad58-4ca7-4be9-8649-0f29e22b81f5
- Product NDC
- 0472-1738
- Form
- SUPPOSITORY
- Composition / generic term
- Miconazole Nitrate
- Labeler
- Actavis Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19950118
- Source listing expiry
- 20261231
Source-listed ingredients
- MICONAZOLE NITRATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 SUPPOSITORY in 1 CARTON (0472-1738-03) · 0472-1738-03
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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