HYDROXYCHLOROQUINE SULFATE
- Product NDC
- 63629-2425
- 11-digit product format
- 636292425
- Labeler code
- 63629
- Product ID
- 63629-2425_86f77857-73e3-4810-8044-eead6b9a10f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxychloroquine sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212902
- Marketing category
- ANDA
- Marketing start
- 2020-07-22
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2425-1 | 63629242501 | 500 TABLET in 1 BOTTLE (63629-2425-1) | 500 tablet | 2021-02-25 | 0000-00-00 | No | No | Current |