Package 51672-4145-6

{"route": ["TOPICAL"], "spl_id": "3c178924-2055-ce8d-e063-6294a90a644f", "openfda": {"nui": ["N0000009267", "N0000009269", "N0000000157"], "upc": ["0351672414566"], "unii": ["P1QW714R7M"], "rxcui": ["310982"], "spl_set_id": ["59af8153-4cf8-4f22-9000-f239798d52d1"], "pharm_class_pe": ["Increased Cytokine Activity [PE]", "Increased Cytokine Production [PE]"], "pharm_class_moa": ["Interferon Inducers [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 PACKET in 1 CARTON (51672-4145-6)  / .25 g in 1 PACKET (51672-4145-8)", "package_ndc": "51672-4145-6", "marketing_start_date": "20110415"}], "brand_name": "Imiquimod", "product_id": "51672-4145_3c178924-2055-ce8d-e063-6294a90a644f", "dosage_form": "CREAM", "pharm_class": ["Increased Cytokine Activity [PE]", "Increased Cytokine Production [PE]", "Interferon Inducers [MoA]"], "product_ndc": "51672-4145", "generic_name": "Imiquimod", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imiquimod", "active_ingredients": [{"name": "IMIQUIMOD", "strength": "50 mg/g"}], "application_number": "ANDA200173", "marketing_category": "ANDA", "marketing_start_date": "20110415", "listing_expiration_date": "20261231"}