| NDC Code | 0591-0698-05 |
|---|
| Package Description | 500 TABLET, COATED in 1 BOTTLE, PLASTIC (0591-0698-05) |
|---|
| Product NDC | 0591-0698 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydroxychloroquine Sulfate |
|---|
| Non-Proprietary Name | Hydroxychloroquine Sulfate |
|---|
| Dosage Form | TABLET, COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19951130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040133 |
|---|
| Manufacturer | Watson Laboratories, Inc. |
|---|
| Substance Name | HYDROXYCHLOROQUINE SULFATE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antirheumatic Agent [EPC] |
|---|