72275-710 NDC - PRILOVIX LITE ()

Drug Information

Product NDC: 72275-710

Proprietary Name: PRILOVIX Lite

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Primary Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	3/17/2019

No.	Package Code	Package Description	Billing Unit
1	72275-710-77	1 PACKAGE in 1 CARTON (72275-710-77) / 15 TUBE in 1 PACKAGE / 1 KIT in 1 TUBE * 30 g in 1 TUBE	EA

Field Name	Field Value	Definition
PRODUCT NDC	72275-710	The 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 NAME	PRILOVIX Lite	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	3/17/2019	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Primary Pharmaceuticals, 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