Package 64950-206-03

{"route": ["ORAL"], "spl_id": "36258c4f-6e18-4fe0-8c35-e77e4d215d94", "openfda": {"upc": ["0364950206036"], "unii": ["NO70W886KK", "68JRS2HC1C"], "rxcui": ["992656", "992668"], "spl_set_id": ["320ff639-9854-407b-9bbd-a035c4f173e1"], "manufacturer_name": ["Genus Lifesciences Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (64950-206-03)", "package_ndc": "64950-206-03", "marketing_start_date": "20220810"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (64950-206-10)", "package_ndc": "64950-206-10", "marketing_start_date": "20220810"}], "brand_name": "Hydrocodone Bitartrate and Homatropine Methylbromide", "product_id": "64950-206_36258c4f-6e18-4fe0-8c35-e77e4d215d94", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "64950-206", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Homatropine Methylbromide", "labeler_name": "Genus Lifesciences Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Homatropine Methylbromide", "active_ingredients": [{"name": "HOMATROPINE METHYLBROMIDE", "strength": "1.5 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "NDA005213", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220810", "listing_expiration_date": "20261231"}