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Acetaminophen and Codeine Phosphate - 63629-3031-2 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 63629-3031
Proprietary Name: Acetaminophen and Codeine Phosphate
Non Proprietary Name: Acetaminophen and Codeine Phosphate
Active Ingredient(s): 300; 60    mg/1; mg/1 & nbsp;   Acetaminophen and Codeine Phosphate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen and Codeine Phosphate

Product NDC: 63629-3031
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040419
Marketing Category: ANDA
Start Marketing Date: 20091117

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 63629-3031-2
Package Description: 120 TABLET in 1 BOTTLE (63629-3031-2)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 63629-3031-2
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 120 TABLET in 1 BOTTLE (63629-3031-2)
Product NDC 63629-3031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091117
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 60
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Acetaminophen and Codeine Phosphate


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