Package 70518-4409-0

Brand: succinylcholine chloride

Generic: succinylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 70518-4409-0
Digits Only 7051844090
Product NDC 70518-4409
Product ID 70518-4409_3b144826-0fef-8a7c-e063-6394a90ad55b
Description

10 VIAL in 1 CARTON (70518-4409-0) / 10 mL in 1 VIAL (70518-4409-1)

Marketing

Marketing Status
Marketed Since 2025-07-29
Brand succinylcholine chloride
Generic succinylcholine chloride
Sample Package No

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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"}