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Acetaminophen And Codeine - 52959-003-12 - (acetaminophen and codeine phosphate)

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Drug Information of Acetaminophen And Codeine

Product NDC: 52959-003
Proprietary Name: Acetaminophen And Codeine
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

Product NDC: 52959-003
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089805
Marketing Category: ANDA
Start Marketing Date: 19880930

Package Information of Acetaminophen And Codeine

Package NDC: 52959-003-12
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (52959-003-12)

NDC Information of Acetaminophen And Codeine

NDC Code 52959-003-12
Proprietary Name Acetaminophen And Codeine
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (52959-003-12)
Product NDC 52959-003
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetaminophen and codeine phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880930
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen And Codeine


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