Metolazone - 68084-418-01 - (Metolazone)

Alphabetical Index


Drug Information of Metolazone

Product NDC: 68084-418
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: 68084-418
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076466
Marketing Category: ANDA
Start Marketing Date: 20101004

Package Information of Metolazone

Package NDC: 68084-418-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-418-01) > 10 TABLET in 1 BLISTER PACK (68084-418-11)

NDC Information of Metolazone

NDC Code 68084-418-01
Proprietary Name Metolazone
Package Description 10 BLISTER PACK in 1 CARTON (68084-418-01) > 10 TABLET in 1 BLISTER PACK (68084-418-11)
Product NDC 68084-418
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metolazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101004
Marketing Category Name ANDA
Labeler Name American Health Packaging
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