HYDROXYCHLOROQUINE SULFATE

Product NDC

72189-085

11-digit product format

721890085

Labeler code

72189

Product ID

72189-085_a189bf91-97ec-233a-e053-2a95a90a9f77

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

HYDROXYCHLOROQUINE SULFATE

Dosage form

TABLET

Route

ORAL

Labeler

DIRECT RX

Application

ANDA201691

Marketing category

ANDA

Marketing start

2020-03-23

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

2021-12-31

Current FDA listing

Historical FDA.report record