Package 0703-0018-01

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0703-0018-01
Digits Only 0703001801
Product NDC 0703-0018
Product ID 0703-0018_c32108cc-7b73-4921-9f9e-54b3d60c1c6e
Description

1 VIAL in 1 CARTON (0703-0018-01) / 50 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2011-01-18
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": "c32108cc-7b73-4921-9f9e-54b3d60c1c6e", "openfda": {"upc": ["0307030110038"], "unii": ["L960UP2KRW"], "rxcui": ["1724338", "1724340", "1724341"], "spl_set_id": ["f0b78db9-a38c-41bb-8233-5e93f7f18c5c"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0703-0018-01)  / 50 mL in 1 VIAL", "package_ndc": "0703-0018-01", "marketing_start_date": "20110118"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "0703-0018_c32108cc-7b73-4921-9f9e-54b3d60c1c6e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0703-0018", "dea_schedule": "CII", "generic_name": "HYDROMORPHONE HYDROCHLORIDE", "labeler_name": "Teva Parenteral Medicines, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA078591", "marketing_category": "ANDA", "marketing_start_date": "20110118", "listing_expiration_date": "20261231"}