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butalbital, acetaminophen and caffeine - 68788-9711-9 - (butalbital, acetaminophen and caffeine)

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Drug Information of butalbital, acetaminophen and caffeine

Product NDC: 68788-9711
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: 68788-9711
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089175
Marketing Category: ANDA
Start Marketing Date: 20130130

Package Information of butalbital, acetaminophen and caffeine

Package NDC: 68788-9711-9
Package Description: 90 TABLET in 1 BOTTLE (68788-9711-9)

NDC Information of butalbital, acetaminophen and caffeine

NDC Code 68788-9711-9
Proprietary Name butalbital, acetaminophen and caffeine
Package Description 90 TABLET in 1 BOTTLE (68788-9711-9)
Product NDC 68788-9711
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name butalbital, acetaminophen and caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130130
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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]

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