Details for New Drug Application (NDA): 218159
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NDA 218159 describes TRAVOPROST, which is a drug marketed by Alembic, Apotex, Chartwell Rx, Gland Pharma Ltd, Lupin Ltd, Micro Labs, Mylan, and Somerset Theraps Llc, and is included in eight NDAs. It is available from seven suppliers. Additional details are available on the TRAVOPROST profile page.
The generic ingredient in TRAVOPROST is travoprost. There are fifteen drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the travoprost profile page.
The generic ingredient in TRAVOPROST is travoprost. There are fifteen drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the travoprost profile page.
Summary for 218159
| Tradename: | TRAVOPROST |
| Applicant: | Gland Pharma Ltd |
| Ingredient: | travoprost |
| Patents: | 0 |
Suppliers and Packaging for NDA: 218159
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| TRAVOPROST | travoprost | SOLUTION/DROPS;OPHTHALMIC | 218159 | ANDA | Gland Pharma Limited | 68083-601 | 68083-601-01 | 1 BOTTLE in 1 CARTON (68083-601-01) / 2.5 mL in 1 BOTTLE |
| TRAVOPROST | travoprost | SOLUTION/DROPS;OPHTHALMIC | 218159 | ANDA | Gland Pharma Limited | 68083-602 | 68083-602-01 | 1 BOTTLE in 1 CARTON (68083-602-01) / 5 mL in 1 BOTTLE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION/DROPS;OPHTHALMIC | Strength | 0.004% | ||||
| Approval Date: | Jul 12, 2024 | TE: | AT | RLD: | No | ||||
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