succinylcholine chloride
Generic: succinylcholine chloride
Labeler: devatis, inc.Drug Facts
Product Profile
Brand Name
succinylcholine chloride
Generic Name
succinylcholine chloride
Labeler
devatis, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
succinylcholine chloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
73043-021
Product ID
73043-021_69451f63-4c69-4774-a791-71257b8794ae
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214491
Listing Expiration
2026-12-31
Marketing Start
2024-09-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73043021
Hyphenated Format
73043-021
Supplemental Identifiers
RxCUI
UPC
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
ANDA214491 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 CARTON (73043-021-01) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "69451f63-4c69-4774-a791-71257b8794ae", "openfda": {"upc": ["0373043021012"], "unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["e235eb7d-5ce2-4884-9d16-493c90d7beba"], "manufacturer_name": ["Devatis, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (73043-021-01) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "73043-021-01", "marketing_start_date": "20240915"}], "brand_name": "Succinylcholine Chloride", "product_id": "73043-021_69451f63-4c69-4774-a791-71257b8794ae", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "73043-021", "generic_name": "Succinylcholine Chloride", "labeler_name": "Devatis, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA214491", "marketing_category": "ANDA", "marketing_start_date": "20240915", "listing_expiration_date": "20261231"}