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Acetaminophen and Codeine - 50436-3227-2 - (Acetaminophen and Codeine)

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Drug Information of Acetaminophen and Codeine

Product NDC: 50436-3227
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: 50436-3227
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040779
Marketing Category: ANDA
Start Marketing Date: 20080529

Package Information of Acetaminophen and Codeine

Package NDC: 50436-3227-2
Package Description: 20 TABLET in 1 BOTTLE (50436-3227-2)

NDC Information of Acetaminophen and Codeine

NDC Code 50436-3227-2
Proprietary Name Acetaminophen and Codeine
Package Description 20 TABLET in 1 BOTTLE (50436-3227-2)
Product NDC 50436-3227
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 Unit Dose Services
Substance Name ACETAMINOPHEN; CODEINE
Strength Number 300; 30
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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