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Acetaminophen and Codeine Phosphate - 17856-0079-2 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 17856-0079
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: 17856-0079
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040119
Marketing Category: ANDA
Start Marketing Date: 19960426

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 17856-0079-2
Package Description: 10 mL in 1 CUP (17856-0079-2)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 17856-0079-2
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 10 mL in 1 CUP (17856-0079-2)
Product NDC 17856-0079
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19960426
Marketing Category Name ANDA
Labeler Name Atlantic Biologicals Corps
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


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