NDC Code | 69238-1544-5 |
Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (69238-1544-5) |
Product NDC | 69238-1544 |
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 | 20180517 |
Marketing Category Name | ANDA |
Application Number | ANDA210577 |
Manufacturer | Amneal Pharmaceuticals NY LLC |
Substance Name | HYDROXYCHLOROQUINE SULFATE |
Strength | 200 |
Strength Unit | mg/1 |
Pharmacy Classes | Antimalarial [EPC], Antirheumatic Agent [EPC] |