Home > National Drug Code (NDC) > Acetaminophen And Codeine

Acetaminophen And Codeine - 33261-002-15 - (acetaminophen and codeine phosphate)

Alphabetical Index


Drug Information of Acetaminophen And Codeine

Product NDC: 33261-002
Proprietary Name: Acetaminophen And Codeine
Non Proprietary Name: acetaminophen and codeine phosphate
Active Ingredient(s): 300; 60    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: 33261-002
Labeler Name: Aidarex Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089828
Marketing Category: ANDA
Start Marketing Date: 19880930

Package Information of Acetaminophen And Codeine

Package NDC: 33261-002-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC (33261-002-15)

NDC Information of Acetaminophen And Codeine

NDC Code 33261-002-15
Proprietary Name Acetaminophen And Codeine
Package Description 15 TABLET in 1 BOTTLE, PLASTIC (33261-002-15)
Product NDC 33261-002
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 Aidarex Pharmaceuticals LLC
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 60
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Acetaminophen And Codeine


General Information