Package 49884-899-11

{"route": ["SUBLINGUAL"], "spl_id": "d2373932-da6e-4cf7-857d-46899fda3063", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["1232194", "1232202"], "spl_set_id": ["44b34e58-114b-4774-9fab-4b188dfe0228"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (49884-899-11)  / 1 TABLET in 1 POUCH (49884-899-52)", "package_ndc": "49884-899-11", "marketing_start_date": "20170911"}], "brand_name": "Zolpidem tartrate sublingual", "product_id": "49884-899_d2373932-da6e-4cf7-857d-46899fda3063", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "49884-899", "dea_schedule": "CIV", "generic_name": "Zolpidem tartrate sublingual", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem tartrate sublingual", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "3.5 mg/1"}], "application_number": "ANDA204229", "marketing_category": "ANDA", "marketing_start_date": "20170911", "listing_expiration_date": "20261231"}