| NDC Code | 52565-023-29 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52565-023-29) > 30 mL in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 52565-023 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Betamethasone Dipropionate |
|---|
| Non-Proprietary Name | Betamethasone Dipropionate |
|---|
| Dosage Form | LOTION, AUGMENTED |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20180214 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA206389 |
|---|
| Manufacturer | Teligent Pharma, Inc. |
|---|
| Substance Name | BETAMETHASONE DIPROPIONATE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|