| NDC Code | 0904-5961-61 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-5961-61) |
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| Product NDC | 0904-5961 |
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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 | 20090610 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076502 |
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| Manufacturer | Major Pharmaceuticals |
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| Substance Name | FEXOFENADINE HYDROCHLORIDE |
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| Strength | 30 |
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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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