69975-870 NDC - BLONIL ()

Drug Information

Product NDC: 69975-870

Proprietary Name: Blonil

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Amvilab LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/16/2015

Package Information

No. Package Code Package Description Billing Unit
169975-870-01100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (69975-870-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69975-870The 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 NAMEBlonilThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/16/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAmvilab LLCName 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