Package 84549-301-25

Brand: succinylcholine chloride

Generic: succinylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 84549-301-25
Digits Only 8454930125
Product NDC 84549-301
Product ID 84549-301_3a38da82-be42-0aec-e063-6394a90a47e4
Description

10 mL in 1 VIAL (84549-301-25)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand succinylcholine chloride
Generic succinylcholine chloride
Sample Package No

Linked Drug Pages (1)

Succinylcholine Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3a38da82-be42-0aec-e063-6394a90a47e4", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["386a63e7-d062-a4c7-e063-6394a90ae77c"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL (84549-301-25)", "package_ndc": "84549-301-25", "marketing_start_date": "20250827"}], "brand_name": "Succinylcholine Chloride", "product_id": "84549-301_3a38da82-be42-0aec-e063-6394a90a47e4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "84549-301", "generic_name": "Succinylcholine Chloride", "labeler_name": "ProPharma Distribution", "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": "20200115", "listing_expiration_date": "20261231"}