0115-4222 NDC - MIDODRINE HYDROCHLORIDE ()

Drug Information

Product NDC: 0115-4222

Proprietary Name: MIDODRINE HYDROCHLORIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Impax Generics
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/27/2004

Package Information

No. Package Code Package Description Billing Unit
10115-4222-01100 TABLET in 1 BOTTLE (0115-4222-01)EA
20115-4222-02500 TABLET in 1 BOTTLE (0115-4222-02)
30115-4222-031000 TABLET in 1 BOTTLE (0115-4222-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0115-4222The 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 NAMEMIDODRINE 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 DATE5/27/2004This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEImpax GenericsName 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