Package 63629-2532-1

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2532-1
Digits Only 6362925321
Product NDC 63629-2532
Description

6 PACKET in 1 BOX (63629-2532-1) / 1 SUPPOSITORY in 1 PACKET

Marketing

Marketing Status
Marketed Since 2021-04-28
Brand hydromorphone hydrochloride
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "971f9f4c-1e16-40fb-b08f-e5dc1424e2d2", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897749"], "spl_set_id": ["bec32a94-4b79-4bd4-b000-45e9030d3106"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 BOX (63629-2532-1)  / 1 SUPPOSITORY in 1 PACKET", "package_ndc": "63629-2532-1", "marketing_start_date": "20210428"}], "brand_name": "HYDROMORPHONE HYDROCHLORIDE", "product_id": "63629-2532_971f9f4c-1e16-40fb-b08f-e5dc1424e2d2", "dosage_form": "SUPPOSITORY", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-2532", "dea_schedule": "CII", "generic_name": "HYDROMORPHONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROMORPHONE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "3 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19960131", "listing_expiration_date": "20261231"}