36987-1418 NDC - BRUSSELS SPROUT ()

Drug Information

Product NDC: 36987-1418

Proprietary Name: Brussels Sprout

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Nelco Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/29/1972

Package Information

No. Package Code Package Description Billing Unit
136987-1418-15 mL in 1 VIAL, MULTI-DOSE (36987-1418-1)
236987-1418-210 mL in 1 VIAL, MULTI-DOSE (36987-1418-2)
336987-1418-330 mL in 1 VIAL, MULTI-DOSE (36987-1418-3)
436987-1418-450 mL in 1 VIAL, MULTI-DOSE (36987-1418-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC36987-1418The 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 NAMEBrussels SproutThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/29/1972This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENelco 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: 5/3/2024