Package 0143-9297-01

Brand: dantrolene

Generic: dantrolene
NDC Package

Package Facts

Identity

Package NDC 0143-9297-01
Digits Only 0143929701
Product NDC 0143-9297
Product ID 0143-9297_769b1f03-2d55-42b7-b29d-60fb5275a67f
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9297-01)

Marketing

Marketing Status
Marketed Since 2017-06-19
Brand dantrolene
Generic dantrolene
Sample Package No

Linked Drug Pages (1)

Dantrolene ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "769b1f03-2d55-42b7-b29d-60fb5275a67f", "openfda": {"unii": ["287M0347EV"], "rxcui": ["856696"], "spl_set_id": ["ab0efc75-0598-4f4e-91ad-6195bb2661fe"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9297-01)", "package_ndc": "0143-9297-01", "marketing_start_date": "20170619"}], "brand_name": "Dantrolene", "product_id": "0143-9297_769b1f03-2d55-42b7-b29d-60fb5275a67f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "0143-9297", "generic_name": "Dantrolene", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dantrolene", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA204762", "marketing_category": "ANDA", "marketing_start_date": "20170619", "listing_expiration_date": "20261231"}