Package 43066-007-10

Brand: rocuronium bromide

Generic: rocuronium bromide
NDC Package

Package Facts

Identity

Package NDC 43066-007-10
Digits Only 4306600710
Product NDC 43066-007
Description

10 VIAL in 1 CARTON (43066-007-10) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2019-07-15
Brand rocuronium bromide
Generic rocuronium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9e0317de-2d78-4fd8-8926-4c7b476f3ed4", "openfda": {"unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["31e15c3f-aefa-4379-b684-7707744fe40d"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (43066-007-10)  / 5 mL in 1 VIAL", "package_ndc": "43066-007-10", "marketing_start_date": "20190715"}], "brand_name": "Rocuronium Bromide", "product_id": "43066-007_9e0317de-2d78-4fd8-8926-4c7b476f3ed4", "dosage_form": "INJECTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "43066-007", "generic_name": "Rocuronium Bromide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rocuronium Bromide", "active_ingredients": [{"name": "ROCURONIUM BROMIDE", "strength": "50 mg/5mL"}], "application_number": "ANDA091115", "marketing_category": "ANDA", "marketing_start_date": "20190715", "listing_expiration_date": "20261231"}