Hydroxychloroquine Sulfate

Product NDC

0904-6508

11-digit product format

009046508

Labeler code

0904

Product ID

0904-6508_cbcf32dd-e40d-4340-8e28-67d947dd3b33

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA040104

Marketing category

ANDA

Marketing start

1995-11-30

Marketing end

0000-00-00

Substance

HYDROXYCHLOROQUINE SULFATE

Active strength

200 mg/1

Pharmacologic classes

Antirheumatic Agent [EPC],Antimalarial [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record