Diurex - 52389-306-42 - (Caffeine, magnesium salicylate)

Alphabetical Index


Drug Information of Diurex

Product NDC: 52389-306
Proprietary Name: Diurex
Non Proprietary Name: Caffeine, magnesium salicylate
Active Ingredient(s): 50; 162.5    mg/1; mg/1 & nbsp;   Caffeine, magnesium salicylate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diurex

Product NDC: 52389-306
Labeler Name: Alva-Amco Pharmacal Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050515

Package Information of Diurex

Package NDC: 52389-306-42
Package Description: 1 BLISTER PACK in 1 CARTON (52389-306-42) > 42 TABLET, COATED in 1 BLISTER PACK (52389-306-01)

NDC Information of Diurex

NDC Code 52389-306-42
Proprietary Name Diurex
Package Description 1 BLISTER PACK in 1 CARTON (52389-306-42) > 42 TABLET, COATED in 1 BLISTER PACK (52389-306-01)
Product NDC 52389-306
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Caffeine, magnesium salicylate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20050515
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Alva-Amco Pharmacal Companies, Inc.
Substance Name CAFFEINE; MAGNESIUM SALICYLATE
Strength Number 50; 162.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Diurex


General Information