Package 0173-0933-08

{"route": ["ORAL"], "spl_id": "753fde77-5750-4c98-a167-daa531f3d872", "openfda": {"upc": ["0301730933089"], "unii": ["G447S0T1VC"], "rxcui": ["108780", "212448", "313564", "313565"], "spl_set_id": ["f8e0d8f8-cb73-4206-a484-88f5c4fbd719"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0173-0933-08)", "package_ndc": "0173-0933-08", "marketing_start_date": "19950801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0173-0933-10)", "package_ndc": "0173-0933-10", "marketing_start_date": "19950801"}], "brand_name": "VALTREX", "product_id": "0173-0933_753fde77-5750-4c98-a167-daa531f3d872", "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": "0173-0933", "generic_name": "valacyclovir hydrochloride", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VALTREX", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "NDA020487", "marketing_category": "NDA", "marketing_start_date": "19950801", "listing_expiration_date": "20261231"}