Hydroxychloroquine Sulfate

Product NDC
33261-933
11-digit product format
332610933
Labeler code
33261
Product ID
33261-933_ba4280ea-864c-4f79-97f9-7438fa0a6105
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxychloroquine Sulfate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
Application
ANDA040766
Marketing category
ANDA
Marketing start
2009-01-07
Marketing end
0000-00-00
Substance
HYDROXYCHLOROQUINE SULFATE
Active strength
200 mg/1
Pharmacologic classes
Antirheumatic Agent [EPC],Antimalarial [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
33261-933-332020-01-31C16284748780-19d75b9d0-497e-f424-e053-dadaa90a57cec293257e-ecd1-4c41-994e-0fe15dee41d2