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Methyclothiazide
Methyclothiazide - 0378-0160-01 - (methyclothiazide)
Drug Information of Methyclothiazide
| Product NDC: | 0378-0160 |
| Proprietary Name: | Methyclothiazide |
| Non Proprietary Name: | methyclothiazide |
| Active Ingredient(s): | 5 mg/1 & nbsp; methyclothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methyclothiazide
| Product NDC: | 0378-0160 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087672 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120430 |
Package Information of Methyclothiazide
| Package NDC: | 0378-0160-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0378-0160-01) |
NDC Information of Methyclothiazide
| NDC Code | 0378-0160-01 |
| Proprietary Name | Methyclothiazide |
| Package Description | 100 TABLET in 1 BOTTLE (0378-0160-01) |
| Product NDC | 0378-0160 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methyclothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120430 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | METHYCLOTHIAZIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
