Package 62332-352-91

{"route": ["ORAL"], "spl_id": "9d36c4e4-75df-42af-bd04-37ccfe7664a7", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["7c33c1b8-100e-4df8-be8d-de3eed7ced94"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-352-31)", "package_ndc": "62332-352-31", "marketing_start_date": "20200305"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (62332-352-60)", "package_ndc": "62332-352-60", "marketing_start_date": "20200305"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-352-91)", "package_ndc": "62332-352-91", "marketing_start_date": "20200305"}], "brand_name": "Doxycycline Hyclate", "product_id": "62332-352_9d36c4e4-75df-42af-bd04-37ccfe7664a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "62332-352", "generic_name": "Doxycycline Hyclate", "labeler_name": "Alembic Pharmaceuticals Inc.", "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"}