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ACETAMINOPHEN AND CODEINE PHOSPHATE - 54868-0072-8 - (acetaminophen and codeine phosphate)

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Drug Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Product NDC: 54868-0072
Proprietary Name: ACETAMINOPHEN AND CODEINE PHOSPHATE
Non Proprietary Name: acetaminophen and codeine phosphate
Active Ingredient(s): 300; 30    mg/1; mg/1 & nbsp;   acetaminophen and codeine phosphate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Product NDC: 54868-0072
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040419
Marketing Category: ANDA
Start Marketing Date: 20030925

Package Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Package NDC: 54868-0072-8
Package Description: 100 TABLET in 1 BOTTLE (54868-0072-8)

NDC Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

NDC Code 54868-0072-8
Proprietary Name ACETAMINOPHEN AND CODEINE PHOSPHATE
Package Description 100 TABLET in 1 BOTTLE (54868-0072-8)
Product NDC 54868-0072
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetaminophen and codeine phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030925
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of ACETAMINOPHEN AND CODEINE PHOSPHATE


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