Package 0781-9053-95

Brand: anectine

Generic: succinylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 0781-9053-95
Digits Only 0781905395
Product NDC 0781-9053
Description

10 VIAL, MULTI-DOSE in 1 CARTON (0781-9053-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-9053-70)

Marketing

Marketing Status
Marketed Since 2019-06-12
Brand anectine
Generic succinylcholine chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "PARENTERAL"], "spl_id": "24ab36dd-dc6b-4207-a5a9-25c6c60df8dc", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589", "1594591"], "spl_set_id": ["04a4e6f5-6fa1-42e1-a3f9-21fca7786b15"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0781-9053-95)  / 10 mL in 1 VIAL, MULTI-DOSE (0781-9053-70)", "package_ndc": "0781-9053-95", "marketing_start_date": "20190612"}], "brand_name": "Anectine", "product_id": "0781-9053_24ab36dd-dc6b-4207-a5a9-25c6c60df8dc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "0781-9053", "generic_name": "Succinylcholine Chloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anectine", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "NDA008453", "marketing_category": "NDA", "marketing_start_date": "20190612", "listing_expiration_date": "20261231"}