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Butalbital, Acetaminophen and Caffeine - 35356-862-90 - (Butalbital, Acetaminophen, and Caffeine)

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Drug Information of Butalbital, Acetaminophen and Caffeine

Product NDC: 35356-862
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: 35356-862
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040513
Marketing Category: ANDA
Start Marketing Date: 20030825

Package Information of Butalbital, Acetaminophen and Caffeine

Package NDC: 35356-862-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (35356-862-90)

NDC Information of Butalbital, Acetaminophen and Caffeine

NDC Code 35356-862-90
Proprietary Name Butalbital, Acetaminophen and Caffeine
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (35356-862-90)
Product NDC 35356-862
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Butalbital, Acetaminophen, and Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030825
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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