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Acetaminophen and Codeine Phosphate - 68788-0285-9 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 68788-0285
Proprietary Name: Acetaminophen and Codeine Phosphate
Non Proprietary Name: Acetaminophen and Codeine Phosphate
Active Ingredient(s): 300; 30    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: 68788-0285
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088628
Marketing Category: ANDA
Start Marketing Date: 20110317

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 68788-0285-9
Package Description: 90 TABLET in 1 BOTTLE (68788-0285-9)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 68788-0285-9
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 90 TABLET in 1 BOTTLE (68788-0285-9)
Product NDC 68788-0285
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110317
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
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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