Package 51660-998-55

{"route": ["ORAL"], "spl_id": "091c0633-b5d5-462a-8aa0-36ae245dbbbc", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1a1afa95-570d-456e-b436-a0fcfaf68517"], "manufacturer_name": ["OHM LABORATORIES INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51660-998-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "51660-998-30", "marketing_start_date": "20220429"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (51660-998-55)  / 150 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "51660-998-55", "marketing_start_date": "20220429"}], "brand_name": "FEXOFENADINE HYDROCHLORIDE", "product_id": "51660-998_091c0633-b5d5-462a-8aa0-36ae245dbbbc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51660-998", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "OHM LABORATORIES INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FEXOFENADINE HYDROCHLORIDE", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA091567", "marketing_category": "ANDA", "marketing_start_date": "20220429", "listing_expiration_date": "20261231"}