Caffeine - 57344-020-03 - (CAFFEINE)

Alphabetical Index


Drug Information of Caffeine

Product NDC: 57344-020
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: 57344-020
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part340
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121215

Package Information of Caffeine

Package NDC: 57344-020-03
Package Description: 10 BLISTER PACK in 1 CARTON (57344-020-03) > 8 TABLET in 1 BLISTER PACK

NDC Information of Caffeine

NDC Code 57344-020-03
Proprietary Name Caffeine
Package Description 10 BLISTER PACK in 1 CARTON (57344-020-03) > 8 TABLET in 1 BLISTER PACK
Product NDC 57344-020
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CAFFEINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121215
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name CAFFEINE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Caffeine


General Information