Package 46708-783-31

{"route": ["ORAL"], "spl_id": "74bab197-f719-48c0-ac84-c0cf0087b45a", "openfda": {"upc": ["0346708783310", "0346708784317"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831102", "831103", "833217"], "spl_set_id": ["74bab197-f719-48c0-ac84-c0cf0087b45a"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-783-31)", "package_ndc": "46708-783-31", "marketing_start_date": "20251114"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (46708-783-71)", "package_ndc": "46708-783-71", "marketing_start_date": "20251114"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "46708-783_74bab197-f719-48c0-ac84-c0cf0087b45a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "46708-783", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA217633", "marketing_category": "ANDA", "marketing_start_date": "20251114", "listing_expiration_date": "20261231"}