Hydroxychloroquine Sulfate

Product NDC

0615-8218

11-digit product format

006158218

Labeler code

0615

Product ID

0615-8218_0e93a4b7-0b88-49cf-aa6e-839a50d5feb3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA040104

Marketing category

ANDA

Marketing start

2018-07-10

Marketing end

2021-04-30

Substance

HYDROXYCHLOROQUINE SULFATE

Active strength

200 mg/1

Pharmacologic classes

Antirheumatic Agent [EPC],Antimalarial [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record