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Acetaminophen, Caffeine and Dihydrocodeine Bitartrate - 64376-611-01 - (Acetaminophen, Caffeine and Dihydrocodeine Bitartrate)

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Drug Information of Acetaminophen, Caffeine and Dihydrocodeine Bitartrate

Product NDC: 64376-611
Proprietary Name: Acetaminophen, Caffeine and Dihydrocodeine Bitartrate
Non Proprietary Name: Acetaminophen, Caffeine and Dihydrocodeine Bitartrate
Active Ingredient(s): 712.8; 60; 32    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Caffeine and Dihydrocodeine Bitartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen, Caffeine and Dihydrocodeine Bitartrate

Product NDC: 64376-611
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040701
Marketing Category: ANDA
Start Marketing Date: 20070403

Package Information of Acetaminophen, Caffeine and Dihydrocodeine Bitartrate

Package NDC: 64376-611-01
Package Description: 100 TABLET in 1 BOTTLE (64376-611-01)

NDC Information of Acetaminophen, Caffeine and Dihydrocodeine Bitartrate

NDC Code 64376-611-01
Proprietary Name Acetaminophen, Caffeine and Dihydrocodeine Bitartrate
Package Description 100 TABLET in 1 BOTTLE (64376-611-01)
Product NDC 64376-611
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen, Caffeine and Dihydrocodeine Bitartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070403
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, Inc.
Substance Name ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Strength Number 712.8; 60; 32
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient],Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Acetaminophen, Caffeine and Dihydrocodeine Bitartrate


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