| Product NDC: | 68258-8976 | 
| Proprietary Name: | Xalatan | 
| Non Proprietary Name: | latanoprost | 
| Active Ingredient(s): | 50 ug/mL & nbsp; latanoprost | 
| Administration Route(s): | OPHTHALMIC | 
| Dosage Form(s): | SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 68258-8976 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA020597 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 19950320 | 
| Package NDC: | 68258-8976-2 | 
| Package Description: | 2.5 mL in 1 BOTTLE, DROPPER (68258-8976-2) | 
| NDC Code | 68258-8976-2 | 
| Proprietary Name | Xalatan | 
| Package Description | 2.5 mL in 1 BOTTLE, DROPPER (68258-8976-2) | 
| Product NDC | 68258-8976 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | latanoprost | 
| Dosage Form Name | SOLUTION | 
| Route Name | OPHTHALMIC | 
| Start Marketing Date | 19950320 | 
| Marketing Category Name | NDA | 
| Labeler Name | Dispensing Solutions, Inc. | 
| Substance Name | LATANOPROST | 
| Strength Number | 50 | 
| Strength Unit | ug/mL | 
| Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |