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Acetaminophen and Codeine Phosphate - 0121-0504-10 - (ACETAMINOPHEN and CODEINE PHOSPHATE)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 0121-0504
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: 0121-0504
Labeler Name: Pharmaceutical Associates, Inc.
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: 0121-0504-10
Package Description: 10 TRAY in 1 CASE (0121-0504-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 0121-0504-10
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 10 TRAY in 1 CASE (0121-0504-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE
Product NDC 0121-0504
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 Pharmaceutical Associates, 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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