Product NDC: | 49884-044 |
Proprietary Name: | Travoprost Ophthalmic Solution 0.004% |
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: | 49884-044 |
Labeler Name: | Par Pharmaceutical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091340 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130415 |
Package NDC: | 49884-044-48 |
Package Description: | 1 BOTTLE in 1 CARTON (49884-044-48) > 2.5 mL in 1 BOTTLE |
NDC Code | 49884-044-48 |
Proprietary Name | Travoprost Ophthalmic Solution 0.004% |
Package Description | 1 BOTTLE in 1 CARTON (49884-044-48) > 2.5 mL in 1 BOTTLE |
Product NDC | 49884-044 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | travoprost |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130415 |
Marketing Category Name | ANDA |
Labeler Name | Par Pharmaceutical, Inc. |
Substance Name | TRAVOPROST |
Strength Number | .04 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |