| Product NDC: | 52125-470 |
| Proprietary Name: | LATANOPROST |
| Non Proprietary Name: | LATANOPROST |
| Active Ingredient(s): | 50 ug/mL & nbsp; LATANOPROST |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52125-470 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090887 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130612 |
| Package NDC: | 52125-470-01 |
| Package Description: | 2.5 mL in 1 BOTTLE, DROPPER (52125-470-01) |
| NDC Code | 52125-470-01 |
| Proprietary Name | LATANOPROST |
| Package Description | 2.5 mL in 1 BOTTLE, DROPPER (52125-470-01) |
| Product NDC | 52125-470 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LATANOPROST |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20130612 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | LATANOPROST |
| Strength Number | 50 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |