Package 0406-3249-01

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-3249-01
Digits Only 0406324901
Product NDC 0406-3249
Product ID 0406-3249_8c16f6cf-c3d2-458c-9cd1-4fddd7c473a8
Description

100 TABLET in 1 BOTTLE (0406-3249-01)

Marketing

Marketing Status
Marketed Since 2004-12-23
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": "8c16f6cf-c3d2-458c-9cd1-4fddd7c473a8", "openfda": {"upc": ["0031100000010"], "unii": ["L960UP2KRW"], "rxcui": ["897696", "897702", "897710"], "spl_set_id": ["4c5c1cc8-c42b-46e3-ad68-8e22f57101f2"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-3249-01)", "package_ndc": "0406-3249-01", "marketing_start_date": "20041223"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "0406-3249_8c16f6cf-c3d2-458c-9cd1-4fddd7c473a8", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-3249", "dea_schedule": "CII", "generic_name": "hydromorphone hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA076855", "marketing_category": "ANDA", "marketing_start_date": "20041223", "listing_expiration_date": "20261231"}