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Methyldopa and Hydrochlorothiazide
Methyldopa and Hydrochlorothiazide - 0378-0711-10 - (methyldopa and hydrochlorothiazide)
Drug Information of Methyldopa and Hydrochlorothiazide
| Product NDC: | 0378-0711 |
| Proprietary Name: | Methyldopa and Hydrochlorothiazide |
| Non Proprietary Name: | methyldopa and hydrochlorothiazide |
| Active Ingredient(s): | 25; 250 mg/1; mg/1 & nbsp; methyldopa and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methyldopa and Hydrochlorothiazide
| Product NDC: | 0378-0711 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070265 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110513 |
Package Information of Methyldopa and Hydrochlorothiazide
| Package NDC: | 0378-0711-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0711-10) |
NDC Information of Methyldopa and Hydrochlorothiazide
| NDC Code | 0378-0711-10 |
| Proprietary Name | Methyldopa and Hydrochlorothiazide |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0711-10) |
| Product NDC | 0378-0711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methyldopa and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110513 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; METHYLDOPA |
| Strength Number | 25; 250 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
