71309-009 NDC - ALLERGY RELIEF ()

Drug Information

Product NDC: 71309-009

Proprietary Name: Allergy Relief

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Safrel Pharmaceuticals, LLC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/12/2012

Package Information

No. Package Code Package Description Billing Unit
171309-009-011000 TABLET in 1 BOTTLE (71309-009-01)
271309-009-06600 TABLET in 1 BOTTLE (71309-009-06)
371309-009-10100 TABLET in 1 BOTTLE (71309-009-10)
471309-009-301 BOTTLE in 1 CARTON (71309-009-30) / 30 TABLET in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC71309-009The 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 NAMEAllergy ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/12/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESafrel Pharmaceuticals, LLC.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024