Package 60687-590-01

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-590-01
Digits Only 6068759001
Product NDC 60687-590
Product ID 60687-590_4bd4edc0-b58e-cd45-e063-6294a90a779c
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-590-01) / 1 TABLET in 1 BLISTER PACK (60687-590-11)

Marketing

Marketing Status
Marketed Since 2021-05-11
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": "4bd4edc0-b58e-cd45-e063-6294a90a779c", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897696", "897702"], "spl_set_id": ["e4758743-9b2c-4612-8399-ad2db372e2b7"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-590-01)  / 1 TABLET in 1 BLISTER PACK (60687-590-11)", "package_ndc": "60687-590-01", "marketing_start_date": "20210511"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "60687-590_4bd4edc0-b58e-cd45-e063-6294a90a779c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60687-590", "dea_schedule": "CII", "generic_name": "hydromorphone hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA076855", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20271231"}