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Dihydrocodeine Bitartrate, Acetaminophen and Caffeine - 54868-5900-0 - (Dihydrocodeine Bitartrate, Acetaminophen and Caffeine)

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Drug Information of Dihydrocodeine Bitartrate, Acetaminophen and Caffeine

Product NDC: 54868-5900
Proprietary Name: Dihydrocodeine Bitartrate, Acetaminophen and Caffeine
Non Proprietary Name: Dihydrocodeine Bitartrate, Acetaminophen and Caffeine
Active Ingredient(s): 712.8; 60; 32    mg/1; mg/1; mg/1 & nbsp;   Dihydrocodeine Bitartrate, Acetaminophen and Caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dihydrocodeine Bitartrate, Acetaminophen and Caffeine

Product NDC: 54868-5900
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040701
Marketing Category: ANDA
Start Marketing Date: 20080520

Package Information of Dihydrocodeine Bitartrate, Acetaminophen and Caffeine

Package NDC: 54868-5900-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-5900-0)

NDC Information of Dihydrocodeine Bitartrate, Acetaminophen and Caffeine

NDC Code 54868-5900-0
Proprietary Name Dihydrocodeine Bitartrate, Acetaminophen and Caffeine
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-5900-0)
Product NDC 54868-5900
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dihydrocodeine Bitartrate, Acetaminophen and Caffeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080520
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Strength Number 712.8; 60; 32
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Dihydrocodeine Bitartrate, Acetaminophen and Caffeine


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