Product NDC: | 24208-485 |
Proprietary Name: | Dorzolamide HCl |
Non Proprietary Name: | Dorzolamide HCl |
Active Ingredient(s): | 20 mg/mL & nbsp; Dorzolamide HCl |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24208-485 |
Labeler Name: | Bausch & Lomb Incorporated |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090143 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090625 |
Package NDC: | 24208-485-10 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-485-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Code | 24208-485-10 |
Proprietary Name | Dorzolamide HCl |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-485-10) > 10 mL in 1 BOTTLE, DROPPER |
Product NDC | 24208-485 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dorzolamide HCl |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20090625 |
Marketing Category Name | ANDA |
Labeler Name | Bausch & Lomb Incorporated |
Substance Name | DORZOLAMIDE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA] |