50145-222 NDC - HIPOGLOS ()

Drug Information

Product NDC: 50145-222

Proprietary Name: Hipoglos

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Laboratorios Andromaco S.A.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/3/2010

Package Information

No. Package Code Package Description Billing Unit
150145-222-011 TUBE in 1 CARTON (50145-222-01) / 120 g in 1 TUBE
250145-222-021 TUBE in 1 CARTON (50145-222-02) / 100 g in 1 TUBE
350145-222-031 TUBE in 1 CARTON (50145-222-03) / 72 g in 1 TUBE
450145-222-041 TUBE in 1 CARTON (50145-222-04) / 60 g in 1 TUBE
550145-222-051 TUBE in 1 CARTON (50145-222-05) / 5 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC50145-222The 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 NAMEHipoglosThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/3/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELaboratorios Andromaco S.A.Name 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