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Methazolamide
Methazolamide - 0781-1072-01 - (Methazolamide)
Drug Information of Methazolamide
| Product NDC: | 0781-1072 |
| Proprietary Name: | Methazolamide |
| Non Proprietary Name: | Methazolamide |
| Active Ingredient(s): | 25 mg/1 & nbsp; Methazolamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methazolamide
| Product NDC: | 0781-1072 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040036 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930630 |
Package Information of Methazolamide
| Package NDC: | 0781-1072-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0781-1072-01) |
NDC Information of Methazolamide
| NDC Code | 0781-1072-01 |
| Proprietary Name | Methazolamide |
| Package Description | 100 TABLET in 1 BOTTLE (0781-1072-01) |
| Product NDC | 0781-1072 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methazolamide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19930630 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | METHAZOLAMIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
