| NDC Code | 0168-0268-50 |
|---|
| Package Description | 50 g in 1 TUBE (0168-0268-50) |
|---|
| Product NDC | 0168-0268 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Betamethasone Dipropionate |
|---|
| Non-Proprietary Name | Betamethasone Dipropionate |
|---|
| Dosage Form | OINTMENT, AUGMENTED |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 19990622 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA075373 |
|---|
| Manufacturer | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
|---|
| Substance Name | BETAMETHASONE DIPROPIONATE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/g |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|