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Metolazone
Metolazone - 0185-5050-10 - (Metolazone)
Drug Information of Metolazone
| Product NDC: | 0185-5050 |
| 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: | 0185-5050 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076732 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031219 |
Package Information of Metolazone
| Package NDC: | 0185-5050-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0185-5050-10) |
NDC Information of Metolazone
| NDC Code | 0185-5050-10 |
| Proprietary Name | Metolazone |
| Package Description | 1000 TABLET in 1 BOTTLE (0185-5050-10) |
| Product NDC | 0185-5050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metolazone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20031219 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | METOLAZONE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |
