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ACETAMINOPHEN AND CODEINE PHOSPHATE - 21695-242-15 - (acetaminophen and codeine phosphate)

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Drug Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Product NDC: 21695-242
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: 21695-242
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040419
Marketing Category: ANDA
Start Marketing Date: 20090629

Package Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

Package NDC: 21695-242-15
Package Description: 15 TABLET in 1 BOTTLE (21695-242-15)

NDC Information of ACETAMINOPHEN AND CODEINE PHOSPHATE

NDC Code 21695-242-15
Proprietary Name ACETAMINOPHEN AND CODEINE PHOSPHATE
Package Description 15 TABLET in 1 BOTTLE (21695-242-15)
Product NDC 21695-242
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetaminophen and codeine phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090629
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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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