Package 68071-4728-7

{"route": ["ORAL"], "spl_id": "284caa29-0b47-3c88-e063-6394a90a259f", "openfda": {"upc": ["0368071472813"], "unii": ["G447S0T1VC"], "rxcui": ["313564"], "spl_set_id": ["8022eb52-da04-eb0a-e053-2a91aa0a6f87"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (68071-4728-1)", "package_ndc": "68071-4728-1", "marketing_start_date": "20190123"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68071-4728-6)", "package_ndc": "68071-4728-6", "marketing_start_date": "20241105"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (68071-4728-7)", "package_ndc": "68071-4728-7", "marketing_start_date": "20241202"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "68071-4728_284caa29-0b47-3c88-e063-6394a90a259f", "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": "68071-4728", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir Hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA090682", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}