Dutoprol - 0310-1087-30 - (metoprolol succinate and hydrochlorothiazide)

Alphabetical Index


Drug Information of Dutoprol

Product NDC: 0310-1087
Proprietary Name: Dutoprol
Non Proprietary Name: metoprolol succinate and hydrochlorothiazide
Active Ingredient(s): 12.5; 25    mg/1; mg/1 & nbsp;   metoprolol succinate and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Dutoprol

Product NDC: 0310-1087
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021956
Marketing Category: NDA
Start Marketing Date: 20111230

Package Information of Dutoprol

Package NDC: 0310-1087-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0310-1087-30)

NDC Information of Dutoprol

NDC Code 0310-1087-30
Proprietary Name Dutoprol
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0310-1087-30)
Product NDC 0310-1087
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol succinate and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111230
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE
Strength Number 12.5; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Dutoprol


General Information