Package 71399-9939-1

{"route": ["ORAL"], "spl_id": "3f7feae3-45bd-adf8-e063-6294a90aee4d", "openfda": {"upc": ["0371399993915"], "unii": ["H0G9379FGK"], "rxcui": ["308907"], "spl_set_id": ["3f7fe022-aee9-b899-e063-6394a90afb4e"], "manufacturer_name": ["AKRON PHARMA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (71399-9939-1)", "package_ndc": "71399-9939-1", "marketing_start_date": "20250923"}], "brand_name": "Regular Strength Assorted Flavors", "product_id": "71399-9939_3f7feae3-45bd-adf8-e063-6294a90aee4d", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "71399-9939", "generic_name": "Antacid Calcium carbonate", "labeler_name": "AKRON PHARMA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Regular Strength", "brand_name_suffix": "Assorted Flavors", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "500 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}