succinylcholine chloride

Generic: succinylcholine chloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name succinylcholine chloride
Generic Name succinylcholine chloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

succinylcholine chloride 20 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621525
Hyphenated Format 51662-1525

Supplemental Identifiers

RxCUI
1594589
UPC
0343598666112
UNII
I9L0DDD30I

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 10 mL in 1 VIAL, MULTI-DOSE (51662-1525-1)
source: ndc

Packages (1)

Ingredients (1)

succinylcholine chloride (20 mg/mL)

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"}