NDC 50989-335-15 - EmulsiVit E-300

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: 50989-335
Requested NDC: 50989-335-15
Package NDCs from labels: 50989-335-15
Manufacturer: Vedco, Inc.
Effective date: 2024-06-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
EmulsiVit E-300	Vedco, Inc.	2024-06-04	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50989-335-15	EmulsiVit E-300	250 mL in 1 VIAL	INJECTION	250		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50989-335	EMULSIVIT E-300 (D-ALPHA TOCOPHEROL VITAMIN A VITAMIN D3) INJECTION [VEDCO, INC.]	2	1 package rows	20240606_9c19a9d1-b936-45e2-8058-ee698b662d47.zip

Reported adverse events (FAERS/openFDA)#

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