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Metolazone
Metolazone - 0378-6172-10 - (metolazone)
Drug Information of Metolazone
| Product NDC: | 0378-6172 |
| Proprietary Name: | Metolazone |
| Non Proprietary Name: | metolazone |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; metolazone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metolazone
| Product NDC: | 0378-6172 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076698 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100118 |
Package Information of Metolazone
| Package NDC: | 0378-6172-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0378-6172-10) |
NDC Information of Metolazone
| NDC Code | 0378-6172-10 |
| Proprietary Name | Metolazone |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0378-6172-10) |
| Product NDC | 0378-6172 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metolazone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100118 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | METOLAZONE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |
