Hydroxychloroquine Sulfate
- Product NDC
- 16571-687
- 11-digit product format
- 165710687
- Labeler code
- 16571
- Product ID
- 16571-687_2c32b62c-751b-4e5d-af42-c296591740bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- 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 NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16571-687-01 | 16571068701 | 100 TABLET, FILM COATED in 1 BOTTLE (16571-687-01) | 2019-09-05 | 0000-00-00 | No | No | Current |
| 16571-687-50 | 16571068750 | 500 TABLET, FILM COATED in 1 BOTTLE (16571-687-50) | 2019-09-05 | 0000-00-00 | No | No | Current |