NDC 55529-163 - Cefenil RTU

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: 55529-163
Package NDCs from labels: 55529-163-02, 55529-163-04
Manufacturer: Norbrook Laboratories Limited
Effective date: 2022-02-07
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Cefenil RTU - Norbrook Laboratories Limited	Norbrook Laboratories Limited	2022-02-07	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55529-163-02	Cefenil RTU	100 mL in 1 VIAL, GLASS	SUSPENSION	100		3
55529-163-04	Cefenil RTU	250 mL in 1 VIAL, GLASS	SUSPENSION	250		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55529-163	CEFENIL RTU (CEFTIOFUR HYDROCHLORIDE) SUSPENSION [NORBROOK LABORATORIES LIMITED]	3	2 package rows	20220208_5626b9a9-df77-48c0-83fc-710a41f64b44.zip

Reported adverse events (FAERS/openFDA)#

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