Package 68071-3749-6

{"route": ["ORAL"], "spl_id": "3aff1c1b-137c-e7a8-e063-6294a90a0318", "openfda": {"upc": ["0368071374964"], "unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["3aff1f5e-d92b-686b-e063-6294a90a2995"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68071-3749-6)", "package_ndc": "68071-3749-6", "marketing_start_date": "20250728"}], "brand_name": "Valacyclovir", "product_id": "68071-3749_3aff1c1b-137c-e7a8-e063-6294a90a0318", "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": "68071-3749", "generic_name": "Valacyclovir", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203047", "marketing_category": "ANDA", "marketing_start_date": "20150525", "listing_expiration_date": "20261231"}