Hydroxychloroquine sulfate
- Product NDC
- 68071-2332
- 11-digit product format
- 680712332
- Labeler code
- 68071
- Product ID
- 68071-2332_3c6be558-7aab-97e6-e063-6294a90af84f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040657
- Marketing category
- ANDA
- Marketing start
- 2019-10-01
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antimalarial [EPC], Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 8Q2869CNVH | HYDROXYCHLOROQUINE SULFATE | 747-36-4 | HYDROXYCHLOROQUINE SULFATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-2332-1 | 68071233201 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-2332-1) | 2021-01-14 | No | No | Historical |