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Butalbital, Acetaminophen and Caffeine - 68387-520-12 - (BUTALBITAL AND ACETAMINOPHEN AND CAFFEINE)

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Drug Information of Butalbital, Acetaminophen and Caffeine

Product NDC: 68387-520
Proprietary Name: Butalbital, Acetaminophen and Caffeine
Non Proprietary Name: BUTALBITAL AND ACETAMINOPHEN AND CAFFEINE
Active Ingredient(s): 500; 50; 40    mg/1; mg/1; mg/1 & nbsp;   BUTALBITAL AND 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: 68387-520
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040336
Marketing Category: ANDA
Start Marketing Date: 20070829

Package Information of Butalbital, Acetaminophen and Caffeine

Package NDC: 68387-520-12
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (68387-520-12)

NDC Information of Butalbital, Acetaminophen and Caffeine

NDC Code 68387-520-12
Proprietary Name Butalbital, Acetaminophen and Caffeine
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (68387-520-12)
Product NDC 68387-520
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUTALBITAL AND ACETAMINOPHEN AND CAFFEINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070829
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
Substance Name ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Strength Number 500; 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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