Package 70436-030-82

{"route": ["INTRAVENOUS"], "spl_id": "1280dbca-a2d7-49cf-e063-6394a90a7596", "openfda": {"unii": ["927L42J563"], "rxcui": ["1734932"], "spl_set_id": ["889bccd1-3793-40ce-bca2-c8c9cf6b7488"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (70436-030-82)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70436-030-82", "marketing_start_date": "20240301"}], "brand_name": "acyclovir", "product_id": "70436-030_1280dbca-a2d7-49cf-e063-6394a90a7596", "dosage_form": "INJECTION, SOLUTION", "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": "70436-030", "generic_name": "acyclovir", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "acyclovir", "active_ingredients": [{"name": "ACYCLOVIR SODIUM", "strength": "50 mg/mL"}], "application_number": "ANDA218111", "marketing_category": "ANDA", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}