| NDC Code | 82009-045-05 |
|---|
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (82009-045-05) |
|---|
| Product NDC | 82009-045 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydroxychloroquine Sulfate |
|---|
| Non-Proprietary Name | Hydroxychloroquine Sulfate |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220930 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040657 |
|---|
| Manufacturer | Quallent Pharmaceuticals Health LLC |
|---|
| Substance Name | HYDROXYCHLOROQUINE SULFATE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antimalarial [EPC], Antirheumatic Agent [EPC] |
|---|