Package 42023-123-06

Brand: dantrium

Generic: dantrolene sodium
NDC Package

Package Facts

Identity

Package NDC 42023-123-06
Digits Only 4202312306
Product NDC 42023-123
Product ID 42023-123_7635e0c2-de42-44ca-9446-59bc0fc41b19
Description

6 VIAL in 1 CARTON (42023-123-06) / 60 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2009-04-20
Brand dantrium
Generic dantrolene sodium
Sample Package No

Linked Drug Pages (1)

Dantrium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "7635e0c2-de42-44ca-9446-59bc0fc41b19", "openfda": {"unii": ["287M0347EV"], "rxcui": ["856696", "856698"], "spl_set_id": ["4df35098-8702-46be-ac67-30cfdf1aa570"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 VIAL in 1 CARTON (42023-123-06)  / 60 mL in 1 VIAL", "package_ndc": "42023-123-06", "marketing_start_date": "20090420"}], "brand_name": "Dantrium", "product_id": "42023-123_7635e0c2-de42-44ca-9446-59bc0fc41b19", "dosage_form": "INJECTION", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "42023-123", "generic_name": "dantrolene sodium", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dantrium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "20 mg/60mL"}], "application_number": "NDA018264", "marketing_category": "NDA", "marketing_start_date": "20090420", "listing_expiration_date": "20261231"}