Package 65219-274-05

Brand: succinylcholine chloride

Generic: succinylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 65219-274-05
Digits Only 6521927405
Product NDC 65219-274
Description

10 SYRINGE, PLASTIC in 1 CARTON (65219-274-05) / 5 mL in 1 SYRINGE, PLASTIC (65219-274-01)

Marketing

Marketing Status
Marketed Since 2025-06-19
Brand succinylcholine chloride
Generic succinylcholine chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "7652543e-1b4b-40b9-8bc3-6fde0ec823ae", "openfda": {"unii": ["8L0S1G435E"], "rxcui": ["2598128"], "spl_set_id": ["f4d496fb-588f-459d-b218-0fc0ffa2715f"], "manufacturer_name": ["Fresenius Kabi USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE, PLASTIC in 1 CARTON (65219-274-05)  / 5 mL in 1 SYRINGE, PLASTIC (65219-274-01)", "package_ndc": "65219-274-05", "marketing_start_date": "20250619"}], "brand_name": "Succinylcholine Chloride", "product_id": "65219-274_7652543e-1b4b-40b9-8bc3-6fde0ec823ae", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "65219-274", "generic_name": "Succinylcholine Chloride", "labeler_name": "Fresenius Kabi USA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE DIHYDRATE", "strength": "20 mg/mL"}], "application_number": "ANDA217884", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}