Package 51672-4108-6

{"route": ["ORAL"], "spl_id": "288442cd-0f6b-49e1-9acc-d8f613f54810", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052", "312084", "312086"], "spl_set_id": ["29cda698-cfd4-43e1-b69e-884d08d8918a"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51672-4108-0)  / 100 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "51672-4108-0", "marketing_start_date": "20110328"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51672-4108-6)", "package_ndc": "51672-4108-6", "marketing_start_date": "20110328"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51672-4108-8)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "51672-4108-8", "marketing_start_date": "20110328"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "51672-4108_288442cd-0f6b-49e1-9acc-d8f613f54810", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "51672-4108", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA077729", "marketing_category": "ANDA", "marketing_start_date": "20110328", "listing_expiration_date": "20261231"}