Package 70518-2039-1

{"route": ["ORAL"], "spl_id": "499baba0-82b1-4029-e063-6294a90a0297", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["212448", "313564"], "spl_set_id": ["56a62c21-bead-4f3b-a24e-c3fd0b4a732f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2039-1)", "package_ndc": "70518-2039-1", "marketing_start_date": "20230717"}, {"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2039-2)", "package_ndc": "70518-2039-2", "marketing_start_date": "20231002"}], "brand_name": "VALTREX", "product_id": "70518-2039_499baba0-82b1-4029-e063-6294a90a0297", "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": "70518-2039", "generic_name": "valacyclovir hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VALTREX", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "NDA020487", "marketing_category": "NDA", "marketing_start_date": "20190426", "listing_expiration_date": "20271231"}