Hydroxychloroquine Sulfate

Product NDC
63629-3343
11-digit product format
636293343
Labeler code
63629
Product ID
63629-3343_dfd63380-f55d-4d12-8d59-93ef5ae12c3c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxychloroquine Sulfate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA009768
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2014-12-12
Marketing end
2022-10-31
Substance
HYDROXYCHLOROQUINE SULFATE
Active strength
200 mg/1
Pharmacologic classes
Antirheumatic Agent [EPC],Antimalarial [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-3343-163629334301100 TABLET in 1 BOTTLE (63629-3343-1) 100 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-26362933430230 TABLET in 1 BOTTLE (63629-3343-2) 30 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-36362933430360 TABLET in 1 BOTTLE (63629-3343-3) 60 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-463629334304180 TABLET in 1 BOTTLE (63629-3343-4) 180 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-56362933430590 TABLET in 1 BOTTLE (63629-3343-5) 90 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-663629334306120 TABLET in 1 BOTTLE (63629-3343-6) 120 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-76362933430710 TABLET in 1 BOTTLE (63629-3343-7) 10 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-86362933430814 TABLET in 1 BOTTLE (63629-3343-8) 14 tablet2021-12-222022-10-31NoNoCurrent
63629-3343-96362933430920 TABLET in 1 BOTTLE (63629-3343-9) 20 tablet2021-12-222022-10-31NoNoCurrent