Bimatoprost
ANDA 205537, held by Eugia Pharma. Bimatoprost.
- First approved: Oct 6, 2022
- Review: Standard
- Supplements approved: 0
- Complete response letters: 0
Approvals and New Uses
The original application and every efficacy supplement, newest first| Date | Submission | Status | Documents |
|---|---|---|---|
| Oct 6, 2022 | Original application | Approved | None posted |
Products
1 strengths and forms| Product | Active ingredient | Marketing |
|---|---|---|
| Bimatoprost0.03% · solution/drops;ophthalmic | Bimatoprost | Rx |
Identifiers
- Application
- ANDA 205537
- Drugs@FDA
- Overview at FDA
- Company
- Eugia Pharma
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed weekly; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters