| NDC Code | 70954-172-10 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70954-172-10) |
|---|
| Product NDC | 70954-172 |
|---|
| 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 | 20220114 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA214581 |
|---|
| Manufacturer | ANI Pharmaceuticals, Inc. |
|---|
| Substance Name | HYDROXYCHLOROQUINE SULFATE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antimalarial [EPC], Antirheumatic Agent [EPC] |
|---|