Hydroxychloroquine Sulfate
- Product NDC
- 43353-972
- 11-digit product format
- 433530972
- Labeler code
- 43353
- Product ID
- 43353-972_331bced4-a4ba-48d9-99fa-4a5c479529f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040766
- Marketing category
- ANDA
- Marketing start
- 2014-05-19
- 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#