Package 63304-173-30

{"route": ["ORAL"], "spl_id": "fd417a50-69b5-40b4-89fd-58aea77ab547", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0363304173307"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["8224b9c5-5c4b-4dda-bc58-47b6604c2884"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (63304-173-03)", "package_ndc": "63304-173-03", "marketing_start_date": "20180806"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (63304-173-10)", "package_ndc": "63304-173-10", "marketing_start_date": "20180806"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63304-173-30)", "package_ndc": "63304-173-30", "marketing_start_date": "20180806"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63304-173-69)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-173-11)", "package_ndc": "63304-173-69", "marketing_start_date": "20180806"}], "brand_name": "Doxycycline", "product_id": "63304-173_fd417a50-69b5-40b4-89fd-58aea77ab547", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63304-173", "generic_name": "Doxycycline", "labeler_name": "Sun Pharmaceutical Industries Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "150 mg/1"}], "application_number": "ANDA065356", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20261231"}