Package 71872-7166-1
Brand: succinylcholine chloride
Generic: succinylcholine chloridePackage Facts
Identity
Package NDC
71872-7166-1
Digits Only
7187271661
Product NDC
71872-7166
Description
1 VIAL, MULTI-DOSE in 1 BAG (71872-7166-1) / 10 mL in 1 VIAL, MULTI-DOSE
Marketing
Marketing Status
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": "fbbf1c9f-000b-1ef4-e053-6294a90abf53", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["896a4238-667d-45b0-e053-2a95a90a60dd"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (71872-7166-1) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71872-7166-1", "marketing_start_date": "20190513"}], "brand_name": "SUCCINYLCHOLINE CHLORIDE", "product_id": "71872-7166_fbbf1c9f-000b-1ef4-e053-6294a90abf53", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "71872-7166", "generic_name": "SUCCINYLCHOLINE CHLORIDE", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUCCINYLCHOLINE CHLORIDE", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA211432", "marketing_category": "ANDA", "marketing_start_date": "20181120", "listing_expiration_date": "20261231"}