Product NDC: | 16571-140 |
Proprietary Name: | Timolol Maleate |
Non Proprietary Name: | Timolol Maleate |
Active Ingredient(s): | 2.5 mg/mL & nbsp; Timolol Maleate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16571-140 |
Labeler Name: | Pack Pharmaceuticals LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077259 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090216 |
Package NDC: | 16571-140-10 |
Package Description: | 1 BOTTLE in 1 CARTON (16571-140-10) > 10 mL in 1 BOTTLE |
NDC Code | 16571-140-10 |
Proprietary Name | Timolol Maleate |
Package Description | 1 BOTTLE in 1 CARTON (16571-140-10) > 10 mL in 1 BOTTLE |
Product NDC | 16571-140 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Timolol Maleate |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20090216 |
Marketing Category Name | ANDA |
Labeler Name | Pack Pharmaceuticals LLC |
Substance Name | TIMOLOL MALEATE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |