| NDC Code | 0168-0266-15 |
|---|
| Package Description | 15 g in 1 TUBE (0168-0266-15) |
|---|
| Product NDC | 0168-0266 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Betamethasone Dipropionate |
|---|
| Non-Proprietary Name | Betamethasone Dipropionate |
|---|
| Dosage Form | GEL |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20030513 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA075276 |
|---|
| Manufacturer | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
|---|
| Substance Name | BETAMETHASONE DIPROPIONATE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/g |
|---|
| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
|---|