Package 0781-3411-95
Brand: anectine
Generic: succinylcholine chloridePackage Facts
Identity
Package NDC
0781-3411-95
Digits Only
0781341195
Product NDC
0781-3411
Description
10 VIAL, MULTI-DOSE in 1 CARTON (0781-3411-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3411-70)
Marketing
Marketing Status
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": "a92278a9-5ec3-4633-91f7-da179c687203", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589", "1594591"], "spl_set_id": ["a1e5d29f-111e-4a44-addf-beeb6ea81711"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0781-3411-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3411-70)", "package_ndc": "0781-3411-95", "marketing_start_date": "20170622"}], "brand_name": "Anectine", "product_id": "0781-3411_a92278a9-5ec3-4633-91f7-da179c687203", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "0781-3411", "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": "20170622", "listing_expiration_date": "20261231"}