Details for New Drug Application (NDA): 201006
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NDA 201006 describes LATANOPROST, which is a drug marketed by Amring Pharms, Apotex Inc, Bausch And Lomb, Epic Pharma Llc, Eugia Pharma, Fdc Ltd, Ryan Labs, Sandoz, and Somerset, and is included in nine NDAs. It is available from eight suppliers. Additional details are available on the LATANOPROST profile page.
The generic ingredient in LATANOPROST is latanoprost. There are twenty drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the latanoprost profile page.
The generic ingredient in LATANOPROST is latanoprost. There are twenty drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the latanoprost profile page.
Summary for 201006
| Tradename: | LATANOPROST |
| Applicant: | Bausch And Lomb |
| Ingredient: | latanoprost |
| Patents: | 0 |
Suppliers and Packaging for NDA: 201006
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LATANOPROST | latanoprost | SOLUTION/DROPS;OPHTHALMIC | 201006 | ANDA | Bausch & Lomb Incorporated | 24208-463 | 24208-463-25 | 1 BOTTLE in 1 CARTON (24208-463-25) / 2.5 mL in 1 BOTTLE |
| LATANOPROST | latanoprost | SOLUTION/DROPS;OPHTHALMIC | 201006 | ANDA | A-S Medication Solutions | 50090-1920 | 50090-1920-0 | 1 BOTTLE in 1 CARTON (50090-1920-0) / 2.5 mL in 1 BOTTLE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION/DROPS;OPHTHALMIC | Strength | 0.005% | ||||
| Approval Date: | Mar 22, 2011 | TE: | AT | RLD: | No | ||||
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