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ACETAMINOPHEN AND CODEINE PHOSPHATE - 0406-0484-23 - (acetaminophen and codeine phosphate)

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Drug Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Product NDC: 0406-0484
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: 0406-0484
Labeler Name: Mallinckrodt, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040419
Marketing Category: ANDA
Start Marketing Date: 20110706

Package Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Package NDC: 0406-0484-23
Package Description: 1 TABLET in 1 BLISTER PACK (0406-0484-23)

NDC Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

NDC Code 0406-0484-23
Proprietary Name ACETAMINOPHEN AND CODEINE PHOSPHATE
Package Description 1 TABLET in 1 BLISTER PACK (0406-0484-23)
Product NDC 0406-0484
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetaminophen and codeine phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110706
Marketing Category Name ANDA
Labeler Name Mallinckrodt, 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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