| NDC Code | 63304-296-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (63304-296-01) |
|---|
| Product NDC | 63304-296 |
|---|
| 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 | 20090107 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040766 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | HYDROXYCHLOROQUINE SULFATE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antirheumatic Agent [EPC],Antimalarial [EPC] |
|---|