Package 68071-4783-3

{"route": ["ORAL"], "spl_id": "308be6ad-e835-c8de-e063-6394a90af3a4", "openfda": {"upc": ["0368071478334"], "unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["82bac944-417a-0af7-e053-2a91aa0a8674"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4783-3)", "package_ndc": "68071-4783-3", "marketing_start_date": "20190225"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68071-4783-6)", "package_ndc": "68071-4783-6", "marketing_start_date": "20250317"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "68071-4783_308be6ad-e835-c8de-e063-6394a90af3a4", "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": "68071-4783", "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": "500 mg/1"}], "application_number": "ANDA090682", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}