Package 71839-141-10
Brand: rocuronium bromide
Generic: rocuronium bromidePackage Facts
Identity
Package NDC
71839-141-10
Digits Only
7183914110
Product NDC
71839-141
Description
10 VIAL, MULTI-DOSE in 1 CARTON (71839-141-10) / 5 mL in 1 VIAL, MULTI-DOSE (71839-141-01)
Marketing
Marketing Status
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": "1543ea2b-54ab-4088-a72a-5d71854a2dce", "openfda": {"upc": ["0371839142019", "0371839141012"], "unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["1543ea2b-54ab-4088-a72a-5d71854a2dce"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (71839-141-10) / 5 mL in 1 VIAL, MULTI-DOSE (71839-141-01)", "package_ndc": "71839-141-10", "marketing_start_date": "20230712"}], "brand_name": "Rocuronium Bromide", "product_id": "71839-141_1543ea2b-54ab-4088-a72a-5d71854a2dce", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "71839-141", "generic_name": "rocuronium bromide", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rocuronium Bromide", "active_ingredients": [{"name": "ROCURONIUM BROMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA216234", "marketing_category": "ANDA", "marketing_start_date": "20230712", "listing_expiration_date": "20261231"}