Hydroxychloroquine Sulfate

Product NDC

50090-0681

11-digit product format

500900681

Labeler code

50090

Product ID

50090-0681_2a3424e0-0db4-4a29-918c-f129d9d08732

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040766

Marketing category

ANDA

Marketing start

2009-01-07

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