70742-092 NDC - ANAL GLIDE ()

Drug Information

Product NDC: 70742-092

Proprietary Name: anal GLIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Product Max Group Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/15/2016

Package Information

No. Package Code Package Description Billing Unit
170742-092-0160 mL in 1 BOTTLE, PUMP (70742-092-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70742-092The 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 NAMEanal GLIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/15/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEProduct Max Group IncName 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