Caffeine - 59779-226-21 - (Caffeine)

Alphabetical Index


Drug Information of Caffeine

Product NDC: 59779-226
Proprietary Name: Caffeine
Non Proprietary Name: Caffeine
Active Ingredient(s): 200    mg/1 & nbsp;   Caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Caffeine

Product NDC: 59779-226
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part340
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19921121

Package Information of Caffeine

Package NDC: 59779-226-21
Package Description: 1 BLISTER PACK in 1 CARTON (59779-226-21) > 16 TABLET in 1 BLISTER PACK

NDC Information of Caffeine

NDC Code 59779-226-21
Proprietary Name Caffeine
Package Description 1 BLISTER PACK in 1 CARTON (59779-226-21) > 16 TABLET in 1 BLISTER PACK
Product NDC 59779-226
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19921121
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name CAFFEINE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Caffeine


General Information