Hydroxychloroquine Sulfate

Product NDC
71335-1949
11-digit product format
713351949
Labeler code
71335
Product ID
71335-1949_82f2dffd-6320-44e8-b174-5c08a0039cab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxychloroquine Sulfate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA210959
Marketing category
ANDA
Marketing start
2019-09-05
Marketing end
0000-00-00
Substance
HYDROXYCHLOROQUINE SULFATE
Active strength
200 mg/1
Pharmacologic classes
Antimalarial [EPC], Antirheumatic Agent [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1949-171335194901100 TABLET, FILM COATED in 1 BOTTLE (71335-1949-1) 2021-10-140000-00-00NoNoCurrent
71335-1949-27133519490230 TABLET, FILM COATED in 1 BOTTLE (71335-1949-2) 2021-10-140000-00-00NoNoCurrent
71335-1949-37133519490360 TABLET, FILM COATED in 1 BOTTLE (71335-1949-3) 2022-09-280000-00-00NoNoCurrent
71335-1949-471335194904180 TABLET, FILM COATED in 1 BOTTLE (71335-1949-4) 2022-09-280000-00-00NoNoCurrent
71335-1949-57133519490590 TABLET, FILM COATED in 1 BOTTLE (71335-1949-5) 2021-10-220000-00-00NoNoCurrent
71335-1949-671335194906120 TABLET, FILM COATED in 1 BOTTLE (71335-1949-6) 2022-09-280000-00-00NoNoCurrent
71335-1949-77133519490710 TABLET, FILM COATED in 1 BOTTLE (71335-1949-7) 2022-09-280000-00-00NoNoCurrent
71335-1949-87133519490814 TABLET, FILM COATED in 1 BOTTLE (71335-1949-8) 2021-09-160000-00-00NoNoCurrent
71335-1949-97133519490920 TABLET, FILM COATED in 1 BOTTLE (71335-1949-9) 2022-09-280000-00-00NoNoCurrent