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Butalbital, Acetaminophen, and Caffeine - 0527-1695-05 - (Butalbital, Acetaminophen, and Caffeine)

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Drug Information of Butalbital, Acetaminophen, and Caffeine

Product NDC: 0527-1695
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: 0527-1695
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200243
Marketing Category: ANDA
Start Marketing Date: 20120913

Package Information of Butalbital, Acetaminophen, and Caffeine

Package NDC: 0527-1695-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0527-1695-05)

NDC Information of Butalbital, Acetaminophen, and Caffeine

NDC Code 0527-1695-05
Proprietary Name Butalbital, Acetaminophen, and Caffeine
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0527-1695-05)
Product NDC 0527-1695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Butalbital, Acetaminophen, and Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120913
Marketing Category Name ANDA
Labeler Name Lannett Company, 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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