NDC 0061-0214 - Banamine

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: 0061-0214
Package NDCs from labels: 0061-0214-02
Manufacturer: Merck Sharp & Dohme Corp.
Effective date: 2025-04-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Banamine ® (flunixin meglumine paste)	Merck Sharp & Dohme Corp.	2025-04-30	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0061-0214-02	Banamine	30 g in 1 SYRINGE	PASTE	30		10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0061-0214	BANAMINE (FLUNIXIN MEGLUMINE) PASTE [MERCK SHARP & DOHME CORP.]	10	1 package rows	20250503_26d5eb1e-e9f3-4c3f-abb2-fe432cf09353.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Flunixin Meglumine	ACTIVE INGREDIENT	8Y3JK0JW3U	BANAMINE (FLUNIXIN MEGLUMINE) PASTE [MERCK SHARP & DOHME CORP.]	2
Flunixin	ACTIVE MOIETY	356IB1O400	BANAMINE (FLUNIXIN MEGLUMINE) PASTE [MERCK SHARP & DOHME CORP.]	2
Carboxymethylcellulose	INACTIVE INGREDIENT	05JZI7B19X	BANAMINE (FLUNIXIN MEGLUMINE) PASTE [MERCK SHARP & DOHME CORP.]	2
Propylene Glycol	INACTIVE INGREDIENT	6DC9Q167V3	BANAMINE (FLUNIXIN MEGLUMINE) PASTE [MERCK SHARP & DOHME CORP.]	2
Starch, Corn	INACTIVE INGREDIENT	O8232NY3SJ	BANAMINE (FLUNIXIN MEGLUMINE) PASTE [MERCK SHARP & DOHME CORP.]	2
Water	INACTIVE INGREDIENT	059QF0KO0R	BANAMINE (FLUNIXIN MEGLUMINE) PASTE [MERCK SHARP & DOHME CORP.]	2

Reported adverse events (FAERS/openFDA)#

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