42708-074 NDC - LOPERAMIDE HYDROCHLORIDE ()

Drug Information

Product NDC: 42708-074

Proprietary Name: Loperamide Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: QPharma Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/1993

Package Information

No. Package Code Package Description Billing Unit
142708-074-2424 CAPSULE in 1 BOTTLE (42708-074-24)

NDC Record

Field Name Field Value Definition
PRODUCT NDC42708-074The 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 NAMELoperamide HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/1/1993This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEQPharma 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