Package 71839-121-25

Brand: succinylcholine chloride

Generic: succinylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 71839-121-25
Digits Only 7183912125
Product NDC 71839-121
Description

25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25) / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)

Marketing

Marketing Status
Marketed Since 2022-02-07
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": "200064fa-2d8d-40ac-92a2-cba54deef1c9", "openfda": {"upc": ["0371839121014"], "unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["6e6e0ce7-c73c-407f-9678-724425f24976"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25)  / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)", "package_ndc": "71839-121-25", "marketing_start_date": "20220207"}], "brand_name": "Succinylcholine Chloride", "product_id": "71839-121_200064fa-2d8d-40ac-92a2-cba54deef1c9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "71839-121", "generic_name": "Succinylcholine Chloride", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA216003", "marketing_category": "ANDA", "marketing_start_date": "20220207", "listing_expiration_date": "20261231"}