Package 51655-312-25

{"route": ["ORAL"], "spl_id": "48eaefc6-3b41-0111-e063-6294a90abbd5", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["ab1cdbbf-d838-020c-e053-2995a90a0f65"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-312-20)", "package_ndc": "51655-312-20", "marketing_start_date": "20200522"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-312-25)", "package_ndc": "51655-312-25", "marketing_start_date": "20200521"}], "brand_name": "Famotidine", "product_id": "51655-312_48eaefc6-3b41-0111-e063-6294a90abbd5", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51655-312", "generic_name": "Famotidine", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075805", "marketing_category": "ANDA", "marketing_start_date": "20200521", "listing_expiration_date": "20271231"}