86056-250 NDC - MICROSILVER ()

Drug Information

Product NDC: 86056-250

Proprietary Name: Microsilver

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: VetBiotek Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/19/2020

Package Information

No. Package Code Package Description Billing Unit
186056-250-08250 mL in 1 BOTTLE, PLASTIC (86056-250-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC86056-250The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMicrosilverThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/19/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEVetBiotek Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023