0713-0622 NDC - TRIPLE ANTIBIOTIC PLUS ()

Drug Information

Product NDC: 0713-0622

Proprietary Name: Triple Antibiotic Plus

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: G&W Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/28/1998

Package Information

No. Package Code Package Description Billing Unit
10713-0622-3128.4 g in 1 TUBE (0713-0622-31)GM

NDC Record

Field Name Field Value Definition
PRODUCT NDC0713-0622The 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 NAMETriple Antibiotic PlusThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/28/1998This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEG&W Laboratories, 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