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
- 70069-403_93e51046-a2f5-47ab-8aa7-b0d8c9c119eb
- Product NDC
- 70069-403
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Bimatoprost
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190619
- 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 (70069-403-01) / 7.5 mL in 1 BOTTLE · 70069-403-01
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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