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metolazone
metolazone - 65580-645-71 - (metolazone)
Drug Information of metolazone
| Product NDC: | 65580-645 |
| Proprietary Name: | metolazone |
| Non Proprietary Name: | metolazone |
| Active Ingredient(s): | 10 mg/1 & nbsp; metolazone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of metolazone
| Product NDC: | 65580-645 |
| Labeler Name: | Upstate Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017386 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19731127 |
Package Information of metolazone
| Package NDC: | 65580-645-71 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (65580-645-71) |
NDC Information of metolazone
| NDC Code | 65580-645-71 |
| Proprietary Name | metolazone |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (65580-645-71) |
| Product NDC | 65580-645 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metolazone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19731127 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Upstate Pharma, LLC |
| Substance Name | METOLAZONE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |
