| NDC Code | 68788-0382-1 |
|---|
| Package Description | 1 TUBE in 1 CARTON (68788-0382-1) > 15 g in 1 TUBE |
|---|
| Product NDC | 68788-0382 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Betamethasone Dipropionate |
|---|
| Non-Proprietary Name | Betamethasone Dipropionate |
|---|
| Dosage Form | OINTMENT, AUGMENTED |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20130319 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074304 |
|---|
| Manufacturer | Preferred Pharmaceuticals Inc. |
|---|
| Substance Name | BETAMETHASONE DIPROPIONATE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/g |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|