Package 0641-6151-25

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-6151-25
Digits Only 0641615125
Product NDC 0641-6151
Product ID 0641-6151_4c244852-0374-445f-8419-72e8ec359faa
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (0641-6151-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0641-6151-01)

Marketing

Marketing Status
Marketed Since 2018-07-01
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": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "4c244852-0374-445f-8419-72e8ec359faa", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["1724276"], "spl_set_id": ["67e79859-4efc-4ea7-8211-cadf746bc864"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (0641-6151-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (0641-6151-01)", "package_ndc": "0641-6151-25", "marketing_start_date": "20180701"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "0641-6151_4c244852-0374-445f-8419-72e8ec359faa", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6151", "dea_schedule": "CII", "generic_name": "Hydromorphone Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA202159", "marketing_category": "ANDA", "marketing_start_date": "20180701", "listing_expiration_date": "20261231"}