NDC Code | 0168-0267-30 |
Package Description | 30 mL in 1 BOTTLE (0168-0267-30) |
Product NDC | 0168-0267 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Betamethasone Dipropionate |
Non-Proprietary Name | Betamethasone Dipropionate |
Dosage Form | LOTION, AUGMENTED |
Usage | TOPICAL |
Start Marketing Date | 20070521 |
Marketing Category Name | ANDA |
Application Number | ANDA077111 |
Manufacturer | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
Substance Name | BETAMETHASONE DIPROPIONATE |
Strength | .5 |
Strength Unit | mg/mL |
Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |