Home > National Drug Code (NDC) > Acetaminophen and Codeine Phosphate

Acetaminophen and Codeine Phosphate - 54569-1001-0 - (ACETAMINOPHEN and CODEINE PHOSPHATE)

Alphabetical Index


Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 54569-1001
Proprietary Name: Acetaminophen and Codeine Phosphate
Non Proprietary Name: ACETAMINOPHEN and CODEINE PHOSPHATE
Active Ingredient(s): 120; 12    mg/5mL; mg/5mL & nbsp;   ACETAMINOPHEN and CODEINE PHOSPHATE
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen and Codeine Phosphate

Product NDC: 54569-1001
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087508
Marketing Category: ANDA
Start Marketing Date: 19810821

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 54569-1001-0
Package Description: 120 mL in 1 BOTTLE (54569-1001-0)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 54569-1001-0
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 120 mL in 1 BOTTLE (54569-1001-0)
Product NDC 54569-1001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ACETAMINOPHEN and CODEINE PHOSPHATE
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19810821
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 120; 12
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Acetaminophen and Codeine Phosphate


General Information