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Hydroxychloroquine sulfate - 55154-2074-0 - (Hydroxychloroquine sulfate)

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Drug Information of Hydroxychloroquine sulfate

Product NDC: 55154-2074
Proprietary Name: Hydroxychloroquine sulfate
Non Proprietary Name: Hydroxychloroquine sulfate
Active Ingredient(s): 200    mg/1 & nbsp;   Hydroxychloroquine sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxychloroquine sulfate

Product NDC: 55154-2074
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040657
Marketing Category: ANDA
Start Marketing Date: 20080805

Package Information of Hydroxychloroquine sulfate

Package NDC: 55154-2074-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2074-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Hydroxychloroquine sulfate

NDC Code 55154-2074-0
Proprietary Name Hydroxychloroquine sulfate
Package Description 10 BLISTER PACK in 1 BAG (55154-2074-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-2074
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxychloroquine sulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080805
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name HYDROXYCHLOROQUINE SULFATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Hydroxychloroquine sulfate


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