| NDC Code | 51672-1316-1 |
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| Package Description | 1 TUBE in 1 CARTON (51672-1316-1) / 15 g in 1 TUBE |
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| Product NDC | 51672-1316 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Alclometasone Dipropionate |
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| Non-Proprietary Name | Alclometasone Dipropionate |
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| Dosage Form | OINTMENT |
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| Usage | TOPICAL |
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| Start Marketing Date | 20040729 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076730 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | ALCLOMETASONE DIPROPIONATE |
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| Strength | .5 |
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| Strength Unit | mg/g |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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