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Acetaminophen and Codeine Phosphate - 54868-0378-2 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 54868-0378
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: 54868-0378
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087508
Marketing Category: ANDA
Start Marketing Date: 20041019

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 54868-0378-2
Package Description: 473 mL in 1 BOTTLE (54868-0378-2)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 54868-0378-2
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 473 mL in 1 BOTTLE (54868-0378-2)
Product NDC 54868-0378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20041019
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 120; 12
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Acetaminophen and Codeine Phosphate


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