| NDC Code | 51672-3007-1 |
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| Package Description | 1 BOTTLE in 1 CARTON (51672-3007-1) / 10 mL in 1 BOTTLE |
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| Product NDC | 51672-3007 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocortisone And Acetic Acid |
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| Non-Proprietary Name | Hydrocortisone And Acetic Acid |
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| Dosage Form | SOLUTION |
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| Usage | AURICULAR (OTIC) |
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| Start Marketing Date | 20050428 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA088759 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | ACETIC ACID; HYDROCORTISONE |
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| Strength | 20.8; 10.4 |
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| Strength Unit | mg/mL; mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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