| NDC Code | 0168-0266-50 |
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| Package Description | 50 g in 1 TUBE (0168-0266-50) |
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| Product NDC | 0168-0266 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Betamethasone Dipropionate |
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| Non-Proprietary Name | Betamethasone Dipropionate |
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| Dosage Form | GEL |
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| Usage | TOPICAL |
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| Start Marketing Date | 20030513 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075276 |
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| Manufacturer | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
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| Substance Name | BETAMETHASONE DIPROPIONATE |
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| Strength | .5 |
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| Strength Unit | mg/g |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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