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Codeine Sulfate - 0527-1698-01 - (Codeine Sulfate)

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Drug Information of Codeine Sulfate

Product NDC: 0527-1698
Proprietary Name: Codeine Sulfate
Non Proprietary Name: Codeine Sulfate
Active Ingredient(s): 30    mg/1 & nbsp;   Codeine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Codeine Sulfate

Product NDC: 0527-1698
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100618

Package Information of Codeine Sulfate

Package NDC: 0527-1698-01
Package Description: 100 TABLET in 1 BOTTLE (0527-1698-01)

NDC Information of Codeine Sulfate

NDC Code 0527-1698-01
Proprietary Name Codeine Sulfate
Package Description 100 TABLET in 1 BOTTLE (0527-1698-01)
Product NDC 0527-1698
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Codeine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100618
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Lannett Company, Inc.
Substance Name CODEINE SULFATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Codeine Sulfate


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