| NDC Code | 51079-548-20 |
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| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-548-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-548-01) |
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| Product NDC | 51079-548 |
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| Product Type Name | HUMAN OTC 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 | 20110927 |
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| End Marketing Date | 20220228 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077081 |
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| Manufacturer | Mylan Institutional Inc. |
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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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