| NDC Code | 49999-772-90 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-772-90) |
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| Product NDC | 49999-772 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fexofenadine Hydrochloride |
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| Non-Proprietary Name | Fexofenadine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20050801 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA020872 |
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| Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
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| Substance Name | FEXOFENADINE HYDROCHLORIDE |
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| Strength | 180 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
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