Fioricet - 52544-957-05 - (Butalbital, Acetaminophen, and Caffeine)

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Drug Information of Fioricet

Product NDC: 52544-957
Proprietary Name: Fioricet
Non Proprietary Name: Butalbital, Acetaminophen, and Caffeine
Active Ingredient(s): 325; 50; 40    mg/1; mg/1; mg/1 & nbsp;   Butalbital, Acetaminophen, and Caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fioricet

Product NDC: 52544-957
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088616
Marketing Category: ANDA
Start Marketing Date: 19841109

Package Information of Fioricet

Package NDC: 52544-957-05
Package Description: 500 TABLET in 1 BOTTLE (52544-957-05)

NDC Information of Fioricet

NDC Code 52544-957-05
Proprietary Name Fioricet
Package Description 500 TABLET in 1 BOTTLE (52544-957-05)
Product NDC 52544-957
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Butalbital, Acetaminophen, and Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19841109
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Strength Number 325; 50; 40
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Fioricet


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