76413-117 NDC - NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE ()

Drug Information

Product NDC: 76413-117

Proprietary Name: Neomycin and Polymyxin B Sulfates and Hydrocortisone

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Central Texas Community Health Centers
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	8/28/1996

No.	Package Code	Package Description	Billing Unit
1	76413-117-10	1 BOTTLE, DROPPER in 1 CARTON (76413-117-10) / 10 mL in 1 BOTTLE, DROPPER

Field Name	Field Value	Definition
PRODUCT NDC	76413-117	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	Neomycin and Polymyxin B Sulfates and Hydrocortisone	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	8/28/1996	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Central Texas Community Health Centers	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