Hydroxychloroquine Sulfate

Product NDC

21695-486

11-digit product format

216950486

Labeler code

21695

Product ID

21695-486_16ea7eee-51c9-4305-9808-358e3ace31bd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Rebel Distributors Corp

Application

ANDA040766

Marketing category

ANDA

Marketing start

2009-01-07

Marketing end

0000-00-00

Substance

HYDROXYCHLOROQUINE SULFATE

Active strength

200 mg/1

Pharmacologic classes

Antirheumatic Agent [EPC],Antimalarial [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record