50114-6922 NDC - BHI MUCUS ()

Drug Information

Product NDC: 50114-6922

Proprietary Name: BHI Mucus

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Heel Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/31/1993

Package Information

No. Package Code Package Description Billing Unit
150114-6922-2100 TABLET in 1 BOTTLE (50114-6922-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50114-6922The 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 NAMEBHI MucusThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/31/1993This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHeel IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024