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ACETAMINOPHEN AND CODEINE PHOSPHATE - 49999-060-01 - (ACETAMINOPHEN AND CODEINE PHOSPHATE)

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Drug Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Product NDC: 49999-060
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: 49999-060
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040419
Marketing Category: ANDA
Start Marketing Date: 20111215

Package Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Package NDC: 49999-060-01
Package Description: 120 TABLET in 1 BOTTLE (49999-060-01)

NDC Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

NDC Code 49999-060-01
Proprietary Name ACETAMINOPHEN AND CODEINE PHOSPHATE
Package Description 120 TABLET in 1 BOTTLE (49999-060-01)
Product NDC 49999-060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ACETAMINOPHEN AND CODEINE PHOSPHATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111215
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of ACETAMINOPHEN AND CODEINE PHOSPHATE


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