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Acetaminophen And Codeine - 66336-059-12 - (acetaminophen and codeine phosphate)

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Drug Information of Acetaminophen And Codeine

Product NDC: 66336-059
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: 66336-059
Labeler Name: Dispensing Solutions, 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: 66336-059-12
Package Description: 12 TABLET in 1 BOTTLE (66336-059-12)

NDC Information of Acetaminophen And Codeine

NDC Code 66336-059-12
Proprietary Name Acetaminophen And Codeine
Package Description 12 TABLET in 1 BOTTLE (66336-059-12)
Product NDC 66336-059
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 Dispensing Solutions, Inc.
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen And Codeine


General Information