United States · FDA National Drug Code directory
bimatoprost
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
- 62332-511_1da93b09-d4d2-4a87-96f5-727004afef8a
- Product NDC
- 62332-511
- Form
- SOLUTION/ DROPS
- Composition / generic term
- bimatoprost
- Labeler
- Alembic Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200121
- Source listing expiry
- 20261231
Source-listed ingredients
- BIMATOPROST — .3 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (62332-511-03) / 3 mL in 1 BOTTLE · 62332-511-03
- 1 BOTTLE in 1 CARTON (62332-511-05) / 5 mL in 1 BOTTLE · 62332-511-05
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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