Package 61919-066-20

{"route": ["ORAL"], "spl_id": "364a2f8b-adfa-b8ce-e063-6394a90a8f9d", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["cbd7bb49-7a9c-4383-a158-bfc307db0130"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (61919-066-20)", "package_ndc": "61919-066-20", "marketing_start_date": "20150101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (61919-066-60)", "package_ndc": "61919-066-60", "marketing_start_date": "20150101"}], "brand_name": "Valacyclovir", "product_id": "61919-066_364a2f8b-adfa-b8ce-e063-6394a90a8f9d", "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": "61919-066", "generic_name": "Valacyclovir", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA201506", "marketing_category": "ANDA", "marketing_start_date": "20150101", "listing_expiration_date": "20261231"}