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Butalbital, Acetaminophen, and Caffeine - 55154-7452-0 - (Butalbital, Acetaminophen, and Caffeine)

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Drug Information of Butalbital, Acetaminophen, and Caffeine

Product NDC: 55154-7452
Proprietary Name: Butalbital, Acetaminophen, and Caffeine
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 Butalbital, Acetaminophen, and Caffeine

Product NDC: 55154-7452
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089718
Marketing Category: ANDA
Start Marketing Date: 19950612

Package Information of Butalbital, Acetaminophen, and Caffeine

Package NDC: 55154-7452-0
Package Description: 10 POUCH in 1 BAG (55154-7452-0) > 1 TABLET in 1 POUCH

NDC Information of Butalbital, Acetaminophen, and Caffeine

NDC Code 55154-7452-0
Proprietary Name Butalbital, Acetaminophen, and Caffeine
Package Description 10 POUCH in 1 BAG (55154-7452-0) > 1 TABLET in 1 POUCH
Product NDC 55154-7452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Butalbital, Acetaminophen, and Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950612
Marketing Category Name ANDA
Labeler Name Cardinal Health
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 Butalbital, Acetaminophen, and Caffeine


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