Package 61314-245-03

{"route": ["OPHTHALMIC"], "spl_id": "c30e555b-1a79-4c3e-b79d-8c1d950fd832", "openfda": {"unii": ["6X97D2XT0O"], "rxcui": ["308720"], "spl_set_id": ["a73519d5-546c-4377-92ed-0d4be2685d60"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (61314-245-01)  / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "61314-245-01", "marketing_start_date": "20000515"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (61314-245-02)  / 15 mL in 1 BOTTLE, PLASTIC", "package_ndc": "61314-245-02", "marketing_start_date": "20000515"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (61314-245-03)  / 10 mL in 1 BOTTLE, PLASTIC", "package_ndc": "61314-245-03", "marketing_start_date": "20000515"}], "brand_name": "Betaxolol Hydrochloride", "product_id": "61314-245_c30e555b-1a79-4c3e-b79d-8c1d950fd832", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "61314-245", "generic_name": "Betaxolol Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betaxolol Hydrochloride", "active_ingredients": [{"name": "BETAXOLOL HYDROCHLORIDE", "strength": "5.6 mg/mL"}], "application_number": "NDA019270", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20000515", "listing_expiration_date": "20261231"}