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Acetaminophen and Codeine - 65162-033-50 - (Acetaminophen and Codeine)

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Drug Information of Acetaminophen and Codeine

Product NDC: 65162-033
Proprietary Name: Acetaminophen and Codeine
Non Proprietary Name: Acetaminophen and Codeine
Active Ingredient(s): 300; 30    mg/1; mg/1 & nbsp;   Acetaminophen and Codeine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen and Codeine

Product NDC: 65162-033
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040779
Marketing Category: ANDA
Start Marketing Date: 20080529

Package Information of Acetaminophen and Codeine

Package NDC: 65162-033-50
Package Description: 500 TABLET in 1 BOTTLE (65162-033-50)

NDC Information of Acetaminophen and Codeine

NDC Code 65162-033-50
Proprietary Name Acetaminophen and Codeine
Package Description 500 TABLET in 1 BOTTLE (65162-033-50)
Product NDC 65162-033
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080529
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
Substance Name ACETAMINOPHEN; CODEINE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen and Codeine


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