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Dorzolamide Hydrochloride
Dorzolamide Hydrochloride - 50383-232-05 - (Dorzolamide Hydrochloride)
Drug Information of Dorzolamide Hydrochloride
| Product NDC: | 50383-232 |
| Proprietary Name: | Dorzolamide Hydrochloride |
| Non Proprietary Name: | Dorzolamide Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Dorzolamide Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dorzolamide Hydrochloride
| Product NDC: | 50383-232 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077846 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081028 |
Package Information of Dorzolamide Hydrochloride
| Package NDC: | 50383-232-05 |
| Package Description: | 1 BOTTLE in 1 CARTON (50383-232-05) > 5 mL in 1 BOTTLE |
NDC Information of Dorzolamide Hydrochloride
| NDC Code | 50383-232-05 |
| Proprietary Name | Dorzolamide Hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (50383-232-05) > 5 mL in 1 BOTTLE |
| Product NDC | 50383-232 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dorzolamide Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20081028 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | DORZOLAMIDE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA] |
