Metolazone - 0378-6173-10 - (metolazone)

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Drug Information of Metolazone

Product NDC: 0378-6173
Proprietary Name: Metolazone
Non Proprietary Name: metolazone
Active Ingredient(s): 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: 0378-6173
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: 0378-6173-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0378-6173-10)

NDC Information of Metolazone

NDC Code 0378-6173-10
Proprietary Name Metolazone
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0378-6173-10)
Product NDC 0378-6173
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 5
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of Metolazone


General Information