| NDC Code | 72641-004-45 |
|---|
| Package Description | 1 TUBE in 1 CARTON (72641-004-45) / 45 g in 1 TUBE |
|---|
| Product NDC | 72641-004 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Betamethasone Dipropionate Usp, 0.05% |
|---|
| Non-Proprietary Name | Betamethasone Dipropionate Usp, 0.05% |
|---|
| Dosage Form | OINTMENT |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20220218 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA215186 |
|---|
| Manufacturer | Tasman Pharma Inc. |
|---|
| Substance Name | BETAMETHASONE DIPROPIONATE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/g |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|