Product NDC: | 0013-8303 |
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: | 0013-8303 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020597 |
Marketing Category: | NDA |
Start Marketing Date: | 19950320 |
Package NDC: | 0013-8303-01 |
Package Description: | 3 BOTTLE, DROPPER in 1 PACKAGE (0013-8303-01) > 2.5 mL in 1 BOTTLE, DROPPER |
NDC Code | 0013-8303-01 |
Proprietary Name | Xalatan |
Package Description | 3 BOTTLE, DROPPER in 1 PACKAGE (0013-8303-01) > 2.5 mL in 1 BOTTLE, DROPPER |
Product NDC | 0013-8303 |
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 | Pharmacia and Upjohn Company |
Substance Name | LATANOPROST |
Strength Number | 50 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |