Hydroxychloroquine Sulfate

Product NDC

10544-578

11-digit product format

105440578

Labeler code

10544

Product ID

10544-578_0fd8c46a-b0cd-52b3-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Blenheim Pharmacal, Inc.

Application

ANDA040766

Marketing category

ANDA

Marketing start

2013-12-20

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