succinylcholine chloride

Generic: succinylcholine chloride

Labeler: fresenius kabi usa llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name succinylcholine chloride
Generic Name succinylcholine chloride
Labeler fresenius kabi usa llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

succinylcholine chloride dihydrate 20 mg/mL

Manufacturer
Fresenius Kabi USA LLC

Identifiers & Regulatory

Product NDC 65219-274
Product ID 65219-274_7652543e-1b4b-40b9-8bc3-6fde0ec823ae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217884
Listing Expiration 2026-12-31
Marketing Start 2025-06-19

Pharmacologic Class

Classes
depolarizing neuromuscular blocker [epc] neuromuscular depolarizing blockade [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65219274
Hyphenated Format 65219-274

Supplemental Identifiers

RxCUI
2598128
UNII
8L0S1G435E

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name succinylcholine chloride (source: ndc)
Generic Name succinylcholine chloride (source: ndc)
Application Number ANDA217884 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 10 SYRINGE, PLASTIC in 1 CARTON (65219-274-05) / 5 mL in 1 SYRINGE, PLASTIC (65219-274-01)
source: ndc

Packages (1)

Ingredients (1)

succinylcholine chloride dihydrate (20 mg/mL)

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"}