Metolazone - 54868-5119-1 - (Metolazone)

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Drug Information of Metolazone

Product NDC: 54868-5119
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: 54868-5119
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076466
Marketing Category: ANDA
Start Marketing Date: 20040720

Package Information of Metolazone

Package NDC: 54868-5119-1
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (54868-5119-1)

NDC Information of Metolazone

NDC Code 54868-5119-1
Proprietary Name Metolazone
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (54868-5119-1)
Product NDC 54868-5119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metolazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040720
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name METOLAZONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of Metolazone


General Information