80208-111 NDC - DELMA ()

Drug Information

Product NDC: 80208-111

Proprietary Name: Delma

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Delma Global, Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/27/2020

Package Information

No. Package Code Package Description Billing Unit
180208-111-0130 mL in 1 BOTTLE (80208-111-01)
280208-111-0259 mL in 1 BOTTLE (80208-111-02)
380208-111-03236 mL in 1 BOTTLE (80208-111-03)
480208-111-04591 mL in 1 BOTTLE (80208-111-04)
580208-111-051000 mL in 1 BOTTLE (80208-111-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80208-111The 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 NAMEDelmaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/27/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDelma Global, 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