Hydroxychloroquine Sulfate

Product NDC

0143-2128

11-digit product format

001432128

Labeler code

0143

Product ID

0143-2128_a631870d-2d3d-4ade-a23f-23d9a8a22f45

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

West-ward Pharmaceutical Corp

Application

ANDA040760

Marketing category

ANDA

Marketing start

2007-08-15

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

2018-12-31

Current FDA listing

Historical FDA.report record