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Acetaminophen and Codeine Phosphate - 55154-8261-3 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 55154-8261
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: 55154-8261
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088629
Marketing Category: ANDA
Start Marketing Date: 20101007

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 55154-8261-3
Package Description: 30 TABLET in 1 BLISTER PACK (55154-8261-3)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 55154-8261-3
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 30 TABLET in 1 BLISTER PACK (55154-8261-3)
Product NDC 55154-8261
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101007
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 60
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen and Codeine Phosphate


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