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Acetaminophen And Codeine - 10544-100-15 - (acetaminophen and codeine phosphate)

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Drug Information of Acetaminophen And Codeine

Product NDC: 10544-100
Proprietary Name: Acetaminophen And Codeine
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

Product NDC: 10544-100
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089805
Marketing Category: ANDA
Start Marketing Date: 20101008

Package Information of Acetaminophen And Codeine

Package NDC: 10544-100-15
Package Description: 15 TABLET in 1 BOTTLE (10544-100-15)

NDC Information of Acetaminophen And Codeine

NDC Code 10544-100-15
Proprietary Name Acetaminophen And Codeine
Package Description 15 TABLET in 1 BOTTLE (10544-100-15)
Product NDC 10544-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetaminophen and codeine phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101008
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen And Codeine


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