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Butalbital, Acetaminophen, and Caffeine - 0143-1115-30 - (Butalbital, Acetaminophen, and Caffeine)

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Drug Information of Butalbital, Acetaminophen, and Caffeine

Product NDC: 0143-1115
Proprietary Name: Butalbital, Acetaminophen, and Caffeine
Non Proprietary Name: Butalbital, Acetaminophen, and Caffeine
Active Ingredient(s): 500; 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: 0143-1115
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040336
Marketing Category: ANDA
Start Marketing Date: 19990818

Package Information of Butalbital, Acetaminophen, and Caffeine

Package NDC: 0143-1115-30
Package Description: 30 TABLET in 1 BOTTLE (0143-1115-30)

NDC Information of Butalbital, Acetaminophen, and Caffeine

NDC Code 0143-1115-30
Proprietary Name Butalbital, Acetaminophen, and Caffeine
Package Description 30 TABLET in 1 BOTTLE (0143-1115-30)
Product NDC 0143-1115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Butalbital, Acetaminophen, and Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990818
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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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