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Hydroxychloroquine Sulfate - 0781-1407-10 - (Hydroxychloroquine Sulfate)

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Drug Information of Hydroxychloroquine Sulfate

Product NDC: 0781-1407
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: 0781-1407
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040104
Marketing Category: ANDA
Start Marketing Date: 19951130

Package Information of Hydroxychloroquine Sulfate

Package NDC: 0781-1407-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1407-10)

NDC Information of Hydroxychloroquine Sulfate

NDC Code 0781-1407-10
Proprietary Name Hydroxychloroquine Sulfate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1407-10)
Product NDC 0781-1407
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxychloroquine Sulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19951130
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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