Plaquenil - 0024-1562-10 - (Hydroxychloroquine Sulfate)

Alphabetical Index


Drug Information of Plaquenil

Product NDC: 0024-1562
Proprietary Name: Plaquenil
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 Plaquenil

Product NDC: 0024-1562
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009768
Marketing Category: NDA
Start Marketing Date: 19550418

Package Information of Plaquenil

Package NDC: 0024-1562-10
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0024-1562-10)

NDC Information of Plaquenil

NDC Code 0024-1562-10
Proprietary Name Plaquenil
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0024-1562-10)
Product NDC 0024-1562
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxychloroquine Sulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19550418
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name HYDROXYCHLOROQUINE SULFATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Plaquenil


General Information