Package 42367-540-32

Brand: ryanodex dantrolene sodium

Generic: dantrolene sodium
NDC Package

Package Facts

Identity

Package NDC 42367-540-32
Digits Only 4236754032
Product NDC 42367-540
Description

1 VIAL in 1 CARTON (42367-540-32) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2014-07-23
Brand ryanodex dantrolene sodium
Generic dantrolene sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2489f99a-e34f-4773-be47-35ebb68cabfb", "openfda": {"upc": ["0342367540325"], "unii": ["287M0347EV"], "rxcui": ["1544753", "1544758"], "spl_set_id": ["8f7b3ac0-604d-4c78-b545-5e0f8ea3d698"], "manufacturer_name": ["Eagle Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42367-540-32)  / 20 mL in 1 VIAL", "package_ndc": "42367-540-32", "marketing_start_date": "20140723"}], "brand_name": "RYANODEX dantrolene sodium", "product_id": "42367-540_2489f99a-e34f-4773-be47-35ebb68cabfb", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "42367-540", "generic_name": "dantrolene sodium", "labeler_name": "Eagle Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RYANODEX", "brand_name_suffix": "dantrolene sodium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "250 mg/5mL"}], "application_number": "NDA205579", "marketing_category": "NDA", "marketing_start_date": "20140723", "listing_expiration_date": "20261231"}