| NDC Code | 68788-7241-5 |
|---|
| Package Description | 50 g in 1 TUBE (68788-7241-5) |
|---|
| Product NDC | 68788-7241 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Betamethasone Dipropionate |
|---|
| Non-Proprietary Name | Betamethasone Dipropionate |
|---|
| Dosage Form | CREAM |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20180813 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078930 |
|---|
| Manufacturer | Preferred Pharmaceuticals Inc., USA |
|---|
| Substance Name | BETAMETHASONE DIPROPIONATE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/g |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|