Home
>
National Drug Code (NDC)
>
Acetazolamide
Acetazolamide - 68084-401-21 - (Acetazolamide)
Drug Information of Acetazolamide
| Product NDC: | 68084-401 |
| Proprietary Name: | Acetazolamide |
| Non Proprietary Name: | Acetazolamide |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetazolamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetazolamide
| Product NDC: | 68084-401 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040904 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100414 |
Package Information of Acetazolamide
| Package NDC: | 68084-401-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-401-21) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-401-11) |
NDC Information of Acetazolamide
| NDC Code | 68084-401-21 |
| Proprietary Name | Acetazolamide |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-401-21) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-401-11) |
| Product NDC | 68084-401 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetazolamide |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100414 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | ACETAZOLAMIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [Chemical/Ingredient] |
