succinylcholine chloride

Generic: succinylcholine chloride

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

succinylcholine chloride 20 mg/mL

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-613
Product ID 70756-613_3e2c0166-09fa-449e-8cda-2240a841e1df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216127
Listing Expiration 2026-12-31
Marketing Start 2023-02-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70756613
Hyphenated Format 70756-613

Supplemental Identifiers

RxCUI
1594589
UPC
0370756613800
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 ANDA216127 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 10 VIAL, MULTI-DOSE in 1 CARTON (70756-613-10) / 10 mL in 1 VIAL, MULTI-DOSE (70756-613-80)
  • 25 VIAL, MULTI-DOSE in 1 CARTON (70756-613-25) / 10 mL in 1 VIAL, MULTI-DOSE (70756-613-80)
source: ndc

Packages (2)

70756-613-10 10 VIAL, MULTI-DOSE in 1 CARTON (70756-613-10) / 10 mL in 1 VIAL, MULTI-DOSE (70756-613-80) 70756-613-25 25 VIAL, MULTI-DOSE in 1 CARTON (70756-613-25) / 10 mL in 1 VIAL, MULTI-DOSE (70756-613-80)

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": "3e2c0166-09fa-449e-8cda-2240a841e1df", "openfda": {"upc": ["0370756613800"], "unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["3e12657f-0e9b-4323-9f64-5420713da156"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (70756-613-10)  / 10 mL in 1 VIAL, MULTI-DOSE (70756-613-80)", "package_ndc": "70756-613-10", "marketing_start_date": "20230202"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (70756-613-25)  / 10 mL in 1 VIAL, MULTI-DOSE (70756-613-80)", "package_ndc": "70756-613-25", "marketing_start_date": "20230202"}], "brand_name": "Succinylcholine Chloride", "product_id": "70756-613_3e2c0166-09fa-449e-8cda-2240a841e1df", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "70756-613", "generic_name": "Succinylcholine Chloride", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA216127", "marketing_category": "ANDA", "marketing_start_date": "20230202", "listing_expiration_date": "20261231"}