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ACETAMINOPHEN AND CODEINE PHOSPHATE - 24236-009-14 - (acetaminophen and codeine phosphate)

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Drug Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Product NDC: 24236-009
Proprietary Name: ACETAMINOPHEN AND CODEINE PHOSPHATE
Non Proprietary Name: acetaminophen and codeine phosphate
Active Ingredient(s): 300    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: 24236-009
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040419
Marketing Category: ANDA
Start Marketing Date: 20130404

Package Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Package NDC: 24236-009-14
Package Description: 2 TABLET in 1 CARTON (24236-009-14)

NDC Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

NDC Code 24236-009-14
Proprietary Name ACETAMINOPHEN AND CODEINE PHOSPHATE
Package Description 2 TABLET in 1 CARTON (24236-009-14)
Product NDC 24236-009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetaminophen and codeine phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130404
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ACETAMINOPHEN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ACETAMINOPHEN AND CODEINE PHOSPHATE


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