Package 42858-234-01

Brand: dilaudid

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42858-234-01
Digits Only 4285823401
Product NDC 42858-234
Product ID 42858-234_00a91762-5403-413c-b3f8-3b4e73684c4f
Description

100 TABLET in 1 BOTTLE, PLASTIC (42858-234-01)

Marketing

Marketing Status
Marketed Since 2017-05-15
Brand dilaudid
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Dilaudid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "00a91762-5403-413c-b3f8-3b4e73684c4f", "openfda": {"upc": ["0342858234016", "0342858122016", "0342858338011"], "unii": ["L960UP2KRW"], "rxcui": ["897657", "897658", "897696", "897698", "897702", "897704", "897710", "897712"], "spl_set_id": ["d6b40e39-a57e-402c-b4f6-7041e832f837"], "manufacturer_name": ["Rhodes Pharmaceuticals L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (42858-234-01)", "package_ndc": "42858-234-01", "marketing_start_date": "20170515"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (42858-234-50)", "package_ndc": "42858-234-50", "marketing_start_date": "20170515"}], "brand_name": "Dilaudid", "product_id": "42858-234_00a91762-5403-413c-b3f8-3b4e73684c4f", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42858-234", "dea_schedule": "CII", "generic_name": "hydromorphone hydrochloride", "labeler_name": "Rhodes Pharmaceuticals L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dilaudid", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "NDA019892", "marketing_category": "NDA", "marketing_start_date": "20170515", "listing_expiration_date": "20271231"}