Package 63323-808-11

Brand: fentanyl citrate

Generic: fentanyl citrate
NDC Package

Package Facts

Identity

Package NDC 63323-808-11
Digits Only 6332380811
Product NDC 63323-808
Description

10 SYRINGE in 1 CARTON (63323-808-11) / 1 mL in 1 SYRINGE (63323-808-01)

Marketing

Marketing Status
Marketed Since 2020-09-30
Brand fentanyl citrate
Generic fentanyl citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a47a3a31-e293-49d5-b6bc-950303525a64", "openfda": {"unii": ["MUN5LYG46H"], "rxcui": ["2474267", "2474269"], "spl_set_id": ["0c10e465-4117-48ba-a454-23ccb7a3fcc7"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (63323-808-11)  / 1 mL in 1 SYRINGE (63323-808-01)", "package_ndc": "63323-808-11", "marketing_start_date": "20200930"}], "brand_name": "Fentanyl Citrate", "product_id": "63323-808_a47a3a31-e293-49d5-b6bc-950303525a64", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63323-808", "dea_schedule": "CII", "generic_name": "Fentanyl Citrate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fentanyl Citrate", "active_ingredients": [{"name": "FENTANYL CITRATE", "strength": "50 ug/mL"}], "application_number": "ANDA212086", "marketing_category": "ANDA", "marketing_start_date": "20200930", "listing_expiration_date": "20261231"}