succinylcholine chloride
Generic: succinylcholine chloride
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
succinylcholine chloride
Generic Name
succinylcholine chloride
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
succinylcholine chloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1525
Product ID
51662-1525_b972f6e4-4fa0-4c68-e053-2995a90ae11b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210698
Listing Expiration
2026-12-31
Marketing Start
2021-01-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621525
Hyphenated Format
51662-1525
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA210698 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 10 mL in 1 VIAL, MULTI-DOSE (51662-1525-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "b972f6e4-4fa0-4c68-e053-2995a90ae11b", "openfda": {"upc": ["0343598666112"], "unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["b972f6e4-4f9f-4c68-e053-2995a90ae11b"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (51662-1525-1)", "package_ndc": "51662-1525-1", "marketing_start_date": "20210121"}], "brand_name": "SUCCINYLCHOLINE CHLORIDE", "product_id": "51662-1525_b972f6e4-4fa0-4c68-e053-2995a90ae11b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "51662-1525", "generic_name": "SUCCINYLCHOLINE CHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUCCINYLCHOLINE CHLORIDE", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA210698", "marketing_category": "ANDA", "marketing_start_date": "20210121", "listing_expiration_date": "20261231"}