Package 16714-249-01

{"route": ["TOPICAL"], "spl_id": "39809045-c9fe-0fc5-e063-6394a90a60b0", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106303"], "spl_set_id": ["2e508351-eca3-427e-8d16-e840a84db0f5"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (16714-249-01)  / 20 g in 1 TUBE", "package_ndc": "16714-249-01", "marketing_start_date": "20220225"}, {"sample": false, "description": "1 TUBE in 1 CARTON (16714-249-02)  / 45 g in 1 TUBE", "package_ndc": "16714-249-02", "marketing_start_date": "20220225"}], "brand_name": "Tretinoin", "product_id": "16714-249_39809045-c9fe-0fc5-e063-6394a90a60b0", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "16714-249", "generic_name": "tretinoin", "labeler_name": "NORTHSTAR RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".5 mg/g"}], "application_number": "ANDA211644", "marketing_category": "ANDA", "marketing_start_date": "20190125", "listing_expiration_date": "20261231"}