| NDC Code | 68210-0122-1 |
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| Package Description | 100 TABLET in 1 BOTTLE (68210-0122-1) |
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| Product NDC | 68210-0122 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20190321 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210137 |
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| Manufacturer | Spirit Pharmaceuticals 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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