Package 31722-120-01

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-120-01
Digits Only 3172212001
Product NDC 31722-120
Product ID 31722-120_8b32d26f-fcb6-43f3-bfd3-8769e9ca6138
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-120-01)

Marketing

Marketing Status
Marketed Since 2020-09-24
Brand hydromorphone hydrochloride
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

hydromorphone hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8b32d26f-fcb6-43f3-bfd3-8769e9ca6138", "openfda": {"upc": ["0331722121019", "0331722122016", "0331722120012", "0331722119016"], "unii": ["L960UP2KRW"], "rxcui": ["902729", "902736", "902741", "1306898"], "spl_set_id": ["c33e6320-4206-4b69-8cac-ebfc2351b8f2"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-120-01)", "package_ndc": "31722-120-01", "marketing_start_date": "20200924"}], "brand_name": "hydromorphone hydrochloride", "product_id": "31722-120_8b32d26f-fcb6-43f3-bfd3-8769e9ca6138", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-120", "dea_schedule": "CII", "generic_name": "hydromorphone hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "hydromorphone hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "12 mg/1"}], "application_number": "ANDA212133", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}