78985-001 NDC - GENERIC -HAND SANITIZER ()

Drug Information

Product NDC: 78985-001

Proprietary Name: Generic -Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Generic Specialties, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/1/2020

Package Information

No. Package Code Package Description Billing Unit
178985-001-0150 GEL in 1 BOTTLE (78985-001-01)
278985-001-0289 GEL in 1 BOTTLE (78985-001-02)
378985-001-03100 GEL in 1 BOTTLE (78985-001-03)
478985-001-04200 GEL in 1 BOTTLE (78985-001-04)
578985-001-05500 GEL in 1 BOTTLE (78985-001-05)
678985-001-061000 GEL in 1 BOTTLE (78985-001-06)
778985-001-075000 GEL in 1 BOTTLE (78985-001-07)
878985-001-08350 GEL in 1 BOTTLE (78985-001-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC78985-001The 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 NAMEGeneric -Hand SanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGeneric Specialties, 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