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Hydroxychloroquine sulfate - Medication Information

Product NDC Code 65841-633
Drug Name

Hydroxychloroquine sulfate

Type Generic
Pharm Class Antimalarial [EPC],
Antirheumatic Agent [EPC]
Active Ingredients
Hydroxychloroquine sulfate 200 mg/1
Route ORAL
Dosage Form TABLET, FILM COATED
RxCUI drug identifier 979092
Application Number ANDA040657
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
65841-633-01 100 tablet, film coated in 1 bottle (65841-633-01)
65841-633-05 500 tablet, film coated in 1 bottle (65841-633-05)
65841-633-30 10 blister pack in 1 carton (65841-633-30) / 10 tablet, film coated in 1 blister pack
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Spl product data elements

Usually a list of ingredients in a drug product.
Hydroxychloroquine sulfate Hydroxychloroquine sulfate HYDROXYCHLOROQUINE SULFATE HYDROXYCHLOROQUINE DIBASIC CALCIUM PHOSPHATE DIHYDRATE MAGNESIUM STEARATE POLYETHYLENE GLYCOL, UNSPECIFIED POLYVINYL ALCOHOL, UNSPECIFIED TALC TITANIUM DIOXIDE STARCH, CORN WHITE TO OFF-WHITE CAPSULE ZC38

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-633-01 in bottle of 100 tablets Hydroxychloroquine Sulfate Tablets USP, 200 mg R x only 100 tablets Hydroxychloroquine sulfate tablets

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API