Hydroxychloroquine Sulfate

Product NDC

66336-555

11-digit product format

663360555

Labeler code

66336

Product ID

66336-555_450d00fd-2711-4689-9fb3-1e6cac7fafb7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Dispensing Solutions, 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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record