| NDC Code | 51672-1306-6 |
|---|
| Package Description | 1 TUBE in 1 CARTON (51672-1306-6) / 45 g in 1 TUBE |
|---|
| Product NDC | 51672-1306 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Alclometasone Dipropionate |
|---|
| Non-Proprietary Name | Alclometasone Dipropionate |
|---|
| Dosage Form | CREAM |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20050915 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076587 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | ALCLOMETASONE DIPROPIONATE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/g |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|