succinylcholine chloride
Generic: succinylcholine chloride
Labeler: fresenius kabi usa llcDrug Facts
Product Profile
Brand Name
succinylcholine chloride
Generic Name
succinylcholine chloride
Labeler
fresenius kabi usa llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
succinylcholine chloride dihydrate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-276
Product ID
65219-276_fdf858c8-71c8-4870-8e5f-baaeb54cde6d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217885
Listing Expiration
2026-12-31
Marketing Start
2025-06-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219276
Hyphenated Format
65219-276
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA217885 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 10 SYRINGE, PLASTIC in 1 CARTON (65219-276-10) / 10 mL in 1 SYRINGE, PLASTIC (65219-276-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "fdf858c8-71c8-4870-8e5f-baaeb54cde6d", "openfda": {"unii": ["8L0S1G435E"], "rxcui": ["2694114"], "spl_set_id": ["ce12d907-eae4-4fba-b85e-170fac1819c6"], "manufacturer_name": ["Fresenius Kabi USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE, PLASTIC in 1 CARTON (65219-276-10) / 10 mL in 1 SYRINGE, PLASTIC (65219-276-01)", "package_ndc": "65219-276-10", "marketing_start_date": "20250619"}], "brand_name": "Succinylcholine Chloride", "product_id": "65219-276_fdf858c8-71c8-4870-8e5f-baaeb54cde6d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "65219-276", "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": "ANDA217885", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}