| NDC Code |
0517-0720-01 |
| Proprietary Name |
Betamethasone Sodium Phosphate and Betamethasone Acetate |
| Package Description |
1 VIAL, MULTI-DOSE in 1 CARTON (0517-0720-01) > 5 mL in 1 VIAL, MULTI-DOSE |
| Product NDC |
0517-0720 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
Betamethasone Sodium Phosphate and Betamethasone Acetate |
| Dosage Form Name |
INJECTION, SUSPENSION |
| Route Name |
INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR |
| Start Marketing Date |
20100428 |
| Marketing Category Name |
ANDA |
| Labeler Name |
American Regent, Inc. |
| Substance Name |
BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE |
| Strength Number |
3; 3 |
| Strength Unit |
mg/mL; mg/mL |
| Pharmaceutical Classes |
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |