Package 78670-003-67
Brand: revonto
Generic: dantrolene sodiumPackage Facts
Identity
Package NDC
78670-003-67
Digits Only
7867000367
Product NDC
78670-003
Description
6 VIAL, GLASS in 1 CARTON (78670-003-67) / 60 mL in 1 VIAL, GLASS
Marketing
Marketing Status
Brand
revonto
Generic
dantrolene sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e2a8cdae-f253-4b7a-b9ab-c66506106aef", "openfda": {"unii": ["287M0347EV"], "rxcui": ["856696", "1012465"], "spl_set_id": ["f1650487-32bd-4017-b9c2-b38829a531af"], "manufacturer_name": ["USWM, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 VIAL, GLASS in 1 CARTON (78670-003-67) / 60 mL in 1 VIAL, GLASS", "package_ndc": "78670-003-67", "marketing_start_date": "20210409"}], "brand_name": "Revonto", "product_id": "78670-003_e2a8cdae-f253-4b7a-b9ab-c66506106aef", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "78670-003", "generic_name": "dantrolene sodium", "labeler_name": "USWM, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Revonto", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "20 mg/60mL"}], "application_number": "ANDA078378", "marketing_category": "ANDA", "marketing_start_date": "20210409", "listing_expiration_date": "20261231"}