Package 43063-547-01

{"route": ["ORAL"], "spl_id": "42ef2624-a5bf-f4f7-e063-6294a90a1400", "openfda": {"upc": ["0343063547823"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["74e2dd24-5c6e-4dde-a2ab-f2d2e61734d8"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-547-01)", "package_ndc": "43063-547-01", "marketing_start_date": "20190107"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-547-20)", "package_ndc": "43063-547-20", "marketing_start_date": "20141105"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-547-82)", "package_ndc": "43063-547-82", "marketing_start_date": "20200521"}], "brand_name": "Ciprofloxacin", "product_id": "43063-547_42ef2624-a5bf-f4f7-e063-6294a90a1400", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "43063-547", "generic_name": "Ciprofloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}