BC - 0135-0500-24 - (aspirin and caffeine)

Alphabetical Index


Drug Information of BC

Product NDC: 0135-0500
Proprietary Name: BC
Non Proprietary Name: aspirin and caffeine
Active Ingredient(s): 845; 65    mg/1; mg/1 & nbsp;   aspirin and caffeine
Administration Route(s): ORAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of BC

Product NDC: 0135-0500
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100608

Package Information of BC

Package NDC: 0135-0500-24
Package Description: 24 POWDER in 1 CARTON (0135-0500-24)

NDC Information of BC

NDC Code 0135-0500-24
Proprietary Name BC
Package Description 24 POWDER in 1 CARTON (0135-0500-24)
Product NDC 0135-0500
Product Type Name HUMAN OTC DRUG
Non Proprietary Name aspirin and caffeine
Dosage Form Name POWDER
Route Name ORAL
Start Marketing Date 20100608
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name ASPIRIN; CAFFEINE
Strength Number 845; 65
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of BC


General Information