NDC 71839-141-01 - Rocuronium Bromide

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 71839-141
Requested NDC: 71839-141-01
Package NDCs from labels: 71839-141-01, 71839-141-10
Manufacturer: ProPharma Distribution
Effective date: 2025-11-07
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Rocuronium Bromide - ProPharma Distribution	ProPharma Distribution	2025-11-07	HUMAN PRESCRIPTION DRUG LABEL
Rocuronium Bromide - Medical Purchasing Solutions, LLC	Medical Purchasing Solutions, LLC	2025-10-21	HUMAN PRESCRIPTION DRUG LABEL
Rocuronium Bromide - BE Pharmaceuticals Inc. \| Caplin Steriles Limited	BE Pharmaceuticals Inc. \| Caplin Steriles Limited	2023-07-12	Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71839-141-01	Rocuronium Bromide	5 mL in 1 VIAL, MULTI-DOSE	INJECTION, SOLUTION	5		1
71839-141-10	Rocuronium Bromide	10 in 1 CARTON	INJECTION, SOLUTION	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71839-141	ROCURONIUM BROMIDE INJECTION, SOLUTION [BE PHARMACEUTICALS INC.]	1	Current NDC, 2 package rows	20230713_1543ea2b-54ab-4088-a72a-5d71854a2dce.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71839-141-01	ML - Milliliter	71839-141	01f4d0f1-513c-4406-85a1-62c2cc67f126	1	2023-09-05
71839-141-10	ML - Milliliter	71839-141	f45c51fe-b934-408a-b784-97734b7f8b08	1	2023-09-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 47 of 47 · 923 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21	Exact identifier unii: 451W47IQ8X
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13	Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12	Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.