succinylcholine chloride

Generic: succinylcholine chloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name succinylcholine chloride
Generic Name succinylcholine chloride
Labeler remedyrepack inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

succinylcholine chloride 20 mg/mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4409
Product ID 70518-4409_3b144826-0fef-8a7c-e063-6394a90ad55b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211589
Listing Expiration 2026-12-31
Marketing Start 2025-07-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184409
Hyphenated Format 70518-4409

Supplemental Identifiers

RxCUI
1594589
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 ANDA211589 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (70518-4409-0) / 10 mL in 1 VIAL (70518-4409-1)
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": "3b144826-0fef-8a7c-e063-6394a90ad55b", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["efe5a242-5ba0-4b14-844c-206a79850d81"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70518-4409-0)  / 10 mL in 1 VIAL (70518-4409-1)", "package_ndc": "70518-4409-0", "marketing_start_date": "20250729"}], "brand_name": "Succinylcholine Chloride", "product_id": "70518-4409_3b144826-0fef-8a7c-e063-6394a90ad55b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "70518-4409", "generic_name": "Succinylcholine Chloride", "labeler_name": "REMEDYREPACK INC.", "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": "20250729", "listing_expiration_date": "20261231"}