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Neptazane
Neptazane - 48102-015-90 - (methazolamide tablets)
Drug Information of Neptazane
| Product NDC: | 48102-015 |
| Proprietary Name: | Neptazane |
| Non Proprietary Name: | methazolamide tablets |
| Active Ingredient(s): | 50 mg/1 & nbsp; methazolamide tablets |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neptazane
| Product NDC: | 48102-015 |
| Labeler Name: | Fera Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040062 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100622 |
Package Information of Neptazane
| Package NDC: | 48102-015-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (48102-015-90) |
NDC Information of Neptazane
| NDC Code | 48102-015-90 |
| Proprietary Name | Neptazane |
| Package Description | 90 TABLET in 1 BOTTLE (48102-015-90) |
| Product NDC | 48102-015 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methazolamide tablets |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100622 |
| Marketing Category Name | ANDA |
| Labeler Name | Fera Pharmaceuticals |
| Substance Name | METHAZOLAMIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
