Product NDC: | 0065-0260 |
Proprietary Name: | Travatan Z |
Non Proprietary Name: | travoprost |
Active Ingredient(s): | .04 mg/mL & nbsp; travoprost |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0065-0260 |
Labeler Name: | Alcon Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021994 |
Marketing Category: | NDA |
Start Marketing Date: | 20061020 |
Package NDC: | 0065-0260-05 |
Package Description: | 5 mL in 1 BOTTLE (0065-0260-05) |
NDC Code | 0065-0260-05 |
Proprietary Name | Travatan Z |
Package Description | 5 mL in 1 BOTTLE (0065-0260-05) |
Product NDC | 0065-0260 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | travoprost |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20061020 |
Marketing Category Name | NDA |
Labeler Name | Alcon Laboratories, Inc |
Substance Name | TRAVOPROST |
Strength Number | .04 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |