NDC Code | 68788-7327-1 |
Package Description | 5 mL in 1 VIAL, MULTI-DOSE (68788-7327-1) |
Product NDC | 68788-7327 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Readysharp Betamethasone |
Non-Proprietary Name | Betamethasone Sodium Phosphate And Betamethasone Acetate |
Dosage Form | INJECTION, SUSPENSION |
Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR |
Start Marketing Date | 20190312 |
Marketing Category Name | ANDA |
Application Number | ANDA090747 |
Manufacturer | Preferred Pharmaceuticals Inc. |
Substance Name | BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE |
Strength | 3; 3 |
Strength Unit | mg/mL; mg/mL |
Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |