Package 63304-905-77

{"route": ["ORAL"], "spl_id": "744b60c8-568b-4726-881c-68709c30f28a", "openfda": {"upc": ["0363304905304", "0363304904307"], "unii": ["G447S0T1VC"], "rxcui": ["313564", "313565"], "spl_set_id": ["26634bf1-c6d8-4d48-9a4e-845c47df07f8"], "manufacturer_name": ["SUN PHARMACEUTICAL INDUSTRIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (63304-905-03)", "package_ndc": "63304-905-03", "marketing_start_date": "20201219"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63304-905-05)", "package_ndc": "63304-905-05", "marketing_start_date": "20201219"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63304-905-30)", "package_ndc": "63304-905-30", "marketing_start_date": "20201219"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (63304-905-77)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-905-11)", "package_ndc": "63304-905-77", "marketing_start_date": "20201219"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63304-905-90)", "package_ndc": "63304-905-90", "marketing_start_date": "20201219"}], "brand_name": "Valacyclovir", "product_id": "63304-905_744b60c8-568b-4726-881c-68709c30f28a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["DNA Polymerase Inhibitors [MoA]", "Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "63304-905", "generic_name": "Valacyclovir", "labeler_name": "SUN PHARMACEUTICAL INDUSTRIES, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA076588", "marketing_category": "ANDA", "marketing_start_date": "20201219", "listing_expiration_date": "20261231"}