Metolazone - 63739-404-10 - (Metolazone)

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Drug Information of Metolazone

Product NDC: 63739-404
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: 63739-404
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076466
Marketing Category: ANDA
Start Marketing Date: 20061115

Package Information of Metolazone

Package NDC: 63739-404-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-404-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Metolazone

NDC Code 63739-404-10
Proprietary Name Metolazone
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-404-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-404
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metolazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061115
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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