Product NDC: | 0378-9645 |
Proprietary Name: | Latanoprost |
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: | 0378-9645 |
Labeler Name: | Mylan Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA201786 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110322 |
Package NDC: | 0378-9645-53 |
Package Description: | 3 BOTTLE in 1 CARTON (0378-9645-53) > 2.5 mL in 1 BOTTLE |
NDC Code | 0378-9645-53 |
Proprietary Name | Latanoprost |
Package Description | 3 BOTTLE in 1 CARTON (0378-9645-53) > 2.5 mL in 1 BOTTLE |
Product NDC | 0378-9645 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | latanoprost |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110322 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Pharmaceuticals Inc. |
Substance Name | LATANOPROST |
Strength Number | 50 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |