MedPath
FDA Product

Hydroxychloroquine sulfate

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Hydroxychloroquine sulfate

16714-110

Regulatory Information

16714-110

ANDA040657

C73584

December 22, 2023

USA

These highlights do not include all the information needed to use HYDROXYCHLOROQUINE SULFATE TABLETS safely and effectively. See full prescribing information for HYDROXYCHLOROQUINE SULFATE TABLETS. HYDROXYCHLOROQUINE SULFATE Tablets, for oral use Initial U.S. Approval: 1955

HUMAN PRESCRIPTION DRUG LABEL

6

Company Information

Northstar Rx LLC.

830546433

Active Ingredients

POLYVINYL ALCOHOL, UNSPECIFIED

Code: 532B59J990

Class Code: IACT

DIBASIC CALCIUM PHOSPHATE DIHYDRATE

Code: O7TSZ97GEP

Class Code: IACT

POLYETHYLENE GLYCOL, UNSPECIFIED

Code: 3WJQ0SDW1A

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

HYDROXYCHLOROQUINE SULFATE

Quantity: 200 mg in 1 1

Code: 8Q2869CNVH

Class Code: ACTIB

TALC

Code: 7SEV7J4R1U

Class Code: IACT

TITANIUM DIOXIDE

Code: 15FIX9V2JP

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

Active Moieties

HYDROXYCHLOROQUINE

Code: 4QWG6N8QKH

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