metolazone - 65580-643-71 - (metolazone)

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Drug Information of metolazone

Product NDC: 65580-643
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: 65580-643
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: 65580-643-71
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (65580-643-71)

NDC Information of metolazone

NDC Code 65580-643-71
Proprietary Name metolazone
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (65580-643-71)
Product NDC 65580-643
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 2.5
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of metolazone


General Information