HYDROXYCHLOROQUINE SULFATE

Product NDC

61919-132

11-digit product format

619190132

Labeler code

61919

Product ID

61919-132_3fda9074-20e6-639c-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

HYDROXYCHLOROQUINE SULFATE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

DIRECT RX

Application

ANDA040657

Marketing category

ANDA

Marketing start

2014-01-01

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