Hydroxychloroquine Sulfate

Product NDC

51660-296

11-digit product format

516600296

Labeler code

51660

Product ID

51660-296_9a11ba29-50ff-41ae-9d56-9f1fe98ccedd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Ohm Laboratories Inc.

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