Package 46708-352-60

{"route": ["ORAL"], "spl_id": "994cfe3e-3b42-4837-b9fc-c88ba7484e51", "openfda": {"upc": ["0346708352608"], "unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["ec4535a1-69f0-40a2-bcba-11afc75c721d"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-352-31)", "package_ndc": "46708-352-31", "marketing_start_date": "20200305"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (46708-352-60)", "package_ndc": "46708-352-60", "marketing_start_date": "20200305"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-352-91)", "package_ndc": "46708-352-91", "marketing_start_date": "20200305"}], "brand_name": "Doxycycline Hyclate", "product_id": "46708-352_994cfe3e-3b42-4837-b9fc-c88ba7484e51", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "46708-352", "generic_name": "Doxycycline Hyclate", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "20 mg/1"}], "application_number": "ANDA210537", "marketing_category": "ANDA", "marketing_start_date": "20200305", "listing_expiration_date": "20261231"}