| 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: | 49884-044-63 |
| Package Description: | 1 BOTTLE in 1 CARTON (49884-044-63) > 5 mL in 1 BOTTLE |
| NDC Code | 49884-044-63 |
| Proprietary Name | Travoprost Ophthalmic Solution 0.004% |
| Package Description | 1 BOTTLE in 1 CARTON (49884-044-63) > 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] |