Package 72572-172-01

Brand: fentanyl citrate

Generic: fentanyl citrate
NDC Package

Package Facts

Identity

Package NDC 72572-172-01
Digits Only 7257217201
Product NDC 72572-172
Product ID 72572-172_e8032003-8bdf-4d16-9cdf-17ceced80cfe
Description

1 VIAL in 1 CARTON (72572-172-01) / 50 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-10-07
Brand fentanyl citrate
Generic fentanyl citrate
Sample Package No

Linked Drug Pages (1)

Fentanyl Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e8032003-8bdf-4d16-9cdf-17ceced80cfe", "openfda": {"unii": ["MUN5LYG46H"], "rxcui": ["1735003", "1735007", "1735013"], "spl_set_id": ["aacf276b-e133-4199-ad3f-67b894744c04"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (72572-172-01)  / 50 mL in 1 VIAL", "package_ndc": "72572-172-01", "marketing_start_date": "20201007"}], "brand_name": "Fentanyl Citrate", "product_id": "72572-172_e8032003-8bdf-4d16-9cdf-17ceced80cfe", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72572-172", "dea_schedule": "CII", "generic_name": "Fentanyl Citrate", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fentanyl Citrate", "active_ingredients": [{"name": "FENTANYL CITRATE", "strength": "50 ug/mL"}], "application_number": "NDA019101", "marketing_category": "NDA", "marketing_start_date": "20201007", "listing_expiration_date": "20271231"}