Package 87063-038-20

{"route": ["ORAL"], "spl_id": "451ccd08-4749-97a1-e063-6294a90ac5ad", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897696", "897702", "897710"], "spl_set_id": ["18f6f54e-1537-4181-9d07-54ddf881a9ee"], "manufacturer_name": ["ASCLEMED USA INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (87063-038-01)", "package_ndc": "87063-038-01", "marketing_start_date": "20251204"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE, PLASTIC (87063-038-05)", "package_ndc": "87063-038-05", "marketing_start_date": "20251204"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (87063-038-07)", "package_ndc": "87063-038-07", "marketing_start_date": "20251204"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (87063-038-10)", "package_ndc": "87063-038-10", "marketing_start_date": "20251204"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (87063-038-14)", "package_ndc": "87063-038-14", "marketing_start_date": "20251204"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (87063-038-20)", "package_ndc": "87063-038-20", "marketing_start_date": "20251204"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (87063-038-30)", "package_ndc": "87063-038-30", "marketing_start_date": "20251204"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (87063-038-50)", "package_ndc": "87063-038-50", "marketing_start_date": "20251203"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (87063-038-60)", "package_ndc": "87063-038-60", "marketing_start_date": "20251204"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (87063-038-90)", "package_ndc": "87063-038-90", "marketing_start_date": "20251204"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "87063-038_451ccd08-4749-97a1-e063-6294a90ac5ad", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "87063-038", "dea_schedule": "CII", "generic_name": "Hydromorphone Hydrochloride", "labeler_name": "ASCLEMED USA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "NDA019892", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20091123", "listing_expiration_date": "20261231"}