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Acetaminophen and Codeine Phosphate - 68788-0076-4 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 68788-0076
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: 68788-0076
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040119
Marketing Category: ANDA
Start Marketing Date: 20110301

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 68788-0076-4
Package Description: 473 mL in 1 BOTTLE (68788-0076-4)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 68788-0076-4
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 473 mL in 1 BOTTLE (68788-0076-4)
Product NDC 68788-0076
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110301
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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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