Metolazone - 51079-023-20 - (metolazone)

Alphabetical Index


Drug Information of Metolazone

Product NDC: 51079-023
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: 51079-023
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076698
Marketing Category: ANDA
Start Marketing Date: 20110114

Package Information of Metolazone

Package NDC: 51079-023-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-023-20) > 1 TABLET in 1 BLISTER PACK (51079-023-01)

NDC Information of Metolazone

NDC Code 51079-023-20
Proprietary Name Metolazone
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-023-20) > 1 TABLET in 1 BLISTER PACK (51079-023-01)
Product NDC 51079-023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metolazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110114
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
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