| NDC Code | 51672-1364-3 |
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| Package Description | 1 BOTTLE, PUMP in 1 CARTON (51672-1364-3) / 45 g in 1 BOTTLE, PUMP |
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| Product NDC | 51672-1364 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Adapalene And Benzoyl Peroxide |
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| Non-Proprietary Name | Adapalene And Benzoyl Peroxide |
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| Dosage Form | GEL |
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| Usage | TOPICAL |
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| Start Marketing Date | 20180124 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206959 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | ADAPALENE; BENZOYL PEROXIDE |
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| Strength | 1; 25 |
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| Strength Unit | mg/g; mg/g |
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| Pharmacy Classes | Retinoid [EPC], Retinoids [CS] |
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