Tafluprost 00781-6184
Product NDC
00781-6184- Manufacturer
- Sandoz Inc
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- December 5, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA209040
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tafluprost | .0045 mg/.3mL |
Drug Class
Prostaglandin Analog [EPC]Increased Prostaglandin Activity [PE]Prostaglandin Analog [EPC]
Packaging Options(1)
6 POUCH in 1 CARTON (0781-6184-87) / 5 CONTAINER in 1 POUCH (0781-6184-14) / .3 mL in 1 CONTAINER