Package 16571-716-10

{"route": ["ORAL"], "spl_id": "0803af00-9ccd-46e7-b1f6-571ce6674049", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["a63eadda-cabb-4f2c-86f9-2d8b4a2c88f3"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16571-716-01)", "package_ndc": "16571-716-01", "marketing_start_date": "20200923"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16571-716-10)", "package_ndc": "16571-716-10", "marketing_start_date": "20200923"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16571-716-50)", "package_ndc": "16571-716-50", "marketing_start_date": "20200923"}], "brand_name": "Tramadol Hydrochloride", "product_id": "16571-716_0803af00-9ccd-46e7-b1f6-571ce6674049", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "16571-716", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA203494", "marketing_category": "ANDA", "marketing_start_date": "20200923", "listing_expiration_date": "20271231"}