Package 70710-1377-2

Brand: succinylcholine chloride

Generic: succinylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 70710-1377-2
Digits Only 7071013772
Product NDC 70710-1377
Description

25 VIAL, MULTI-DOSE in 1 TRAY (70710-1377-2) / 10 mL in 1 VIAL, MULTI-DOSE (70710-1377-1)

Marketing

Marketing Status
Marketed Since 2018-05-10
Brand succinylcholine chloride
Generic succinylcholine chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "bd190da3-9daf-4859-a431-87c693e18e90", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["017e5ad4-028e-4e34-ac09-d0c8d64c880a"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (70710-1377-2)  / 10 mL in 1 VIAL, MULTI-DOSE (70710-1377-1)", "package_ndc": "70710-1377-2", "marketing_start_date": "20180510"}], "brand_name": "Succinylcholine Chloride", "product_id": "70710-1377_bd190da3-9daf-4859-a431-87c693e18e90", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "70710-1377", "generic_name": "Succinylcholine Chloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA209467", "marketing_category": "ANDA", "marketing_start_date": "20180510", "listing_expiration_date": "20261231"}