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Acetaminophen And Codeine - 0603-2337-28 - (acetaminophen and codeine phosphate)

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Drug Information of Acetaminophen And Codeine

Product NDC: 0603-2337
Proprietary Name: Acetaminophen And Codeine
Non Proprietary Name: acetaminophen and codeine phosphate
Active Ingredient(s): 300; 15    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: 0603-2337
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089990
Marketing Category: ANDA
Start Marketing Date: 19880930

Package Information of Acetaminophen And Codeine

Package NDC: 0603-2337-28
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0603-2337-28)

NDC Information of Acetaminophen And Codeine

NDC Code 0603-2337-28
Proprietary Name Acetaminophen And Codeine
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0603-2337-28)
Product NDC 0603-2337
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 Qualitest Pharmaceuticals
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 15
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Acetaminophen And Codeine


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