Product NDC: | 67877-229 |
Proprietary Name: | Timolol Maleate |
Non Proprietary Name: | Timolol Maleate |
Active Ingredient(s): | 5 mg/mL & nbsp; Timolol Maleate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67877-229 |
Labeler Name: | Ascend Laboratories, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077259 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110309 |
Package NDC: | 67877-229-15 |
Package Description: | 1 BOTTLE, DISPENSING in 1 CARTON (67877-229-15) > 15 mL in 1 BOTTLE, DISPENSING |
NDC Code | 67877-229-15 |
Proprietary Name | Timolol Maleate |
Package Description | 1 BOTTLE, DISPENSING in 1 CARTON (67877-229-15) > 15 mL in 1 BOTTLE, DISPENSING |
Product NDC | 67877-229 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Timolol Maleate |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110309 |
Marketing Category Name | ANDA |
Labeler Name | Ascend Laboratories, LLC |
Substance Name | TIMOLOL MALEATE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |