10888-5006 NDC - AMANTADINE HCL ()

Drug Information

Product NDC: 10888-5006

Proprietary Name: Amantadine HCl

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Banner Pharmacaps Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/1/2012

Package Information

No. Package Code Package Description Billing Unit
110888-5006-2100 CAPSULE, LIQUID FILLED in 1 BOTTLE (10888-5006-2)EA
210888-5006-3500 CAPSULE, LIQUID FILLED in 1 BOTTLE (10888-5006-3)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC10888-5006The 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 NAMEAmantadine HClThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/1/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBanner Pharmacaps 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