succinylcholine chloride

Generic: succinylcholine chloride

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name succinylcholine chloride
Generic Name succinylcholine chloride
Labeler somerset therapeutics, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

succinylcholine chloride 20 mg/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-783
Product ID 70069-783_5c6877a5-1296-4619-9a7c-01dae4ddf5ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211589
Listing Expiration 2026-12-31
Marketing Start 2023-05-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069783
Hyphenated Format 70069-783

Supplemental Identifiers

RxCUI
1594589
UPC
0370069783016
UNII
I9L0DDD30I

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 ANDA211589 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (70069-783-10) / 10 mL in 1 VIAL
  • 25 VIAL in 1 CARTON (70069-783-25) / 10 mL in 1 VIAL
source: ndc

Packages (2)

70069-783-10 10 VIAL in 1 CARTON (70069-783-10) / 10 mL in 1 VIAL 70069-783-25 25 VIAL in 1 CARTON (70069-783-25) / 10 mL in 1 VIAL

Ingredients (1)

succinylcholine chloride (20 mg/mL)

Linked Drug Pages (1)

Succinylcholine Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "5c6877a5-1296-4619-9a7c-01dae4ddf5ac", "openfda": {"upc": ["0370069783016"], "unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["690a0231-dbba-4695-a843-842a14c6587c"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70069-783-10)  / 10 mL in 1 VIAL", "package_ndc": "70069-783-10", "marketing_start_date": "20230530"}, {"sample": false, "description": "25 VIAL in 1 CARTON (70069-783-25)  / 10 mL in 1 VIAL", "package_ndc": "70069-783-25", "marketing_start_date": "20230530"}], "brand_name": "Succinylcholine Chloride", "product_id": "70069-783_5c6877a5-1296-4619-9a7c-01dae4ddf5ac", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "70069-783", "generic_name": "Succinylcholine Chloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA211589", "marketing_category": "ANDA", "marketing_start_date": "20230530", "listing_expiration_date": "20261231"}