77085-100 NDC - ULTRA GUARD ()

Drug Information

Product NDC: 77085-100

Proprietary Name: Ultra Guard

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Midwest extraction services llc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/15/2020

Package Information

No. Package Code Package Description Billing Unit
177085-100-013785 mL in 1 BOTTLE, PLASTIC (77085-100-01)
277085-100-02473 mL in 1 BOTTLE, PUMP (77085-100-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC77085-100The 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 NAMEUltra GuardThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/15/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMidwest extraction services 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