80308-002 NDC - B-PROTEK ()

Drug Information

Product NDC: 80308-002

Proprietary Name: B-Protek

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Grupo Siller Ingenier�a Construcci�n y Materiales, S.A. de C.V
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/24/2020

Package Information

No. Package Code Package Description Billing Unit
180308-002-013 mL in 1 POUCH (80308-002-01)
280308-002-0230 mL in 1 BOTTLE, PLASTIC (80308-002-02)
380308-002-0360 mL in 1 BOTTLE, PLASTIC (80308-002-03)
480308-002-04250 mL in 1 BOTTLE, PLASTIC (80308-002-04)
580308-002-05500 mL in 1 BOTTLE, PLASTIC (80308-002-05)
680308-002-061000 mL in 1 BOTTLE, PLASTIC (80308-002-06)
780308-002-073785 mL in 1 BOTTLE, PLASTIC (80308-002-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80308-002The 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 NAMEB-ProtekThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/24/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGrupo Siller Ingenier�a Construcci�n y Materiales, S.A. de C.VName 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