Hydroxychloroquine Sulfate

Product NDC
71335-1771
11-digit product format
713351771
Labeler code
71335
Product ID
71335-1771_34ede119-f969-48e4-a54a-6050323002a7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxychloroquine Sulfate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040081
Marketing category
ANDA
Marketing start
2020-10-08
Substance
HYDROXYCHLOROQUINE SULFATE
Active strength
200 mg/1
Pharmacologic classes
Antimalarial [EPC], Antirheumatic Agent [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
8Q2869CNVHHYDROXYCHLOROQUINE SULFATE747-36-4HYDROXYCHLOROQUINE SULFATE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-1771-171335177101100 TABLET, FILM COATED in 1 BOTTLE (71335-1771-1) 2021-09-02NoNoHistorical
71335-1771-27133517710230 TABLET, FILM COATED in 1 BOTTLE (71335-1771-2) 2021-08-19NoNoHistorical
71335-1771-37133517710360 TABLET, FILM COATED in 1 BOTTLE (71335-1771-3) 2021-12-29NoNoHistorical
71335-1771-471335177104180 TABLET, FILM COATED in 1 BOTTLE (71335-1771-4) 2021-01-21NoNoHistorical
71335-1771-57133517710590 TABLET, FILM COATED in 1 BOTTLE (71335-1771-5) 2021-12-29NoNoHistorical
71335-1771-671335177106120 TABLET, FILM COATED in 1 BOTTLE (71335-1771-6) 2021-12-29NoNoHistorical
71335-1771-77133517710710 TABLET, FILM COATED in 1 BOTTLE (71335-1771-7) 2021-08-16NoNoHistorical
71335-1771-87133517710814 TABLET, FILM COATED in 1 BOTTLE (71335-1771-8) 2021-12-29NoNoHistorical
71335-1771-97133517710920 TABLET, FILM COATED in 1 BOTTLE (71335-1771-9) 2021-08-18NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Hydroxychloroquine SulfateBryant Ranch Prepack2024-04-05HUMAN PRESCRIPTION DRUG LABEL104