71276-120 NDC - ULTRA REJUVE 7S AMPOULE ()

Drug Information

Product NDC: 71276-120

Proprietary Name: ULTRA REJUVE 7S AMPOULE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ULAB
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/2/2017

Package Information

No. Package Code Package Description Billing Unit
171276-120-025 VIAL in 1 CARTON (71276-120-02) / 5 mL in 1 VIAL (71276-120-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71276-120The 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 REJUVE 7S AMPOULEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/2/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEULABName 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