Hydroxychloroquine Sulfate

Product NDC

16714-474

11-digit product format

167140474

Labeler code

16714

Product ID

16714-474_0fd6ecfd-3e5d-4553-8609-326ef96b27fb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Northstar RxLLC

Application

ANDA040104

Marketing category

ANDA

Marketing start

2015-12-18

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