Package 0904-6565-61

{"route": ["ORAL"], "spl_id": "7a8b6144-8be6-4464-9d93-a95e22eb4a01", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["fd982aee-d503-47b3-8d3d-42e9a8690457"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6565-07)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6565-07", "marketing_start_date": "20100524"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6565-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6565-61", "marketing_start_date": "20100524"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "0904-6565_7a8b6144-8be6-4464-9d93-a95e22eb4a01", "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": "0904-6565", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir Hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA090682", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}