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BUTALBITAL, ACETAMINOPHEN AND CAFFEINE - 16590-581-30 - (BUTALBITAL, ACETAMINOPHEN AND CAFFEINE)

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Drug Information of BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product NDC: 16590-581
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: 16590-581
Labeler Name: STAT RX USA 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: 16590-581-30
Package Description: 30 TABLET in 1 BOTTLE (16590-581-30)

NDC Information of BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

NDC Code 16590-581-30
Proprietary Name BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
Package Description 30 TABLET in 1 BOTTLE (16590-581-30)
Product NDC 16590-581
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 STAT RX USA 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]

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