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Butalbital, Acetaminophen and Caffeine - 54868-1036-3 - (Butalbital, Acetaminophen and Caffeine)

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Drug Information of Butalbital, Acetaminophen and Caffeine

Product NDC: 54868-1036
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: 54868-1036
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089718
Marketing Category: ANDA
Start Marketing Date: 20040621

Package Information of Butalbital, Acetaminophen and Caffeine

Package NDC: 54868-1036-3
Package Description: 50 TABLET in 1 BOTTLE (54868-1036-3)

NDC Information of Butalbital, Acetaminophen and Caffeine

NDC Code 54868-1036-3
Proprietary Name Butalbital, Acetaminophen and Caffeine
Package Description 50 TABLET in 1 BOTTLE (54868-1036-3)
Product NDC 54868-1036
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Butalbital, Acetaminophen and Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040621
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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 Butalbital, Acetaminophen and Caffeine


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