Hydroxychloroquine sulfate

Product NDC

77651-2321

11-digit product format

776512321

Labeler code

77651

Product ID

77651-2321_a75c9a6c-0609-7784-e053-2995a90ad145

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxychloroquine Sulfate

Dosage form

TABLET

Route

ORAL

Labeler

Quifma S.A

Application

ANDA215095

Marketing category

ANDA

Marketing start

2020-08-19

Marketing end

0000-00-00

Substance

HYDROXYCHLOROQUINE

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