Package 0168-0268-15

{"route": ["TOPICAL"], "spl_id": "e6484210-45ae-49f9-9b3a-ff7b309e9bc9", "openfda": {"upc": ["0301680268156"], "unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["853399f8-95a7-41f3-80e7-7ed8e3ff1a5e"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 g in 1 TUBE (0168-0268-15)", "package_ndc": "0168-0268-15", "marketing_start_date": "19990622"}, {"sample": false, "description": "50 g in 1 TUBE (0168-0268-50)", "package_ndc": "0168-0268-50", "marketing_start_date": "19990622"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0168-0268_e6484210-45ae-49f9-9b3a-ff7b309e9bc9", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0268", "generic_name": "betamethasone dipropionate", "labeler_name": "E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA075373", "marketing_category": "ANDA", "marketing_start_date": "19990622", "listing_expiration_date": "20271231"}