Home > National Drug Code (NDC) > Hydroxychloroquine Sulfate

Hydroxychloroquine Sulfate - 21695-486-30 - (Hydroxychloroquine Sulfate)

Alphabetical Index


Drug Information of Hydroxychloroquine Sulfate

Product NDC: 21695-486
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: 21695-486
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040766
Marketing Category: ANDA
Start Marketing Date: 20090107

Package Information of Hydroxychloroquine Sulfate

Package NDC: 21695-486-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-486-30)

NDC Information of Hydroxychloroquine Sulfate

NDC Code 21695-486-30
Proprietary Name Hydroxychloroquine Sulfate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-486-30)
Product NDC 21695-486
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxychloroquine Sulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090107
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name HYDROXYCHLOROQUINE SULFATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Hydroxychloroquine Sulfate


General Information