69276-200 NDC - BRIOSCHI EFFERVESCENT ANTACID ()

Drug Information

Product NDC: 69276-200

Proprietary Name: Brioschi Effervescent Antacid

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Pharmacy Class(es):

Increased Large Intestinal Motility [PE];
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
Osmotic Activity [MoA];
Osmotic Laxative [EPC]

Labeler Information

Labeler Name:	Neobourne Pharma LP
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	6/5/2017
End Marketing Date:	3/31/2023

Package Information

No.	Package Code	Package Description
1	69276-200-05	10 PACKET in 1 CARTON (69276-200-05) / 5 g in 1 PACKET
2	69276-200-25	240 g in 1 BOTTLE (69276-200-25)
3	69276-200-58	300 g in 1 BOTTLE (69276-200-58)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	69276-200	The 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 NAME	Brioschi Effervescent Antacid	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	11/27/2017	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Neobourne Pharma LP	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	69276-200	The 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 NAME	Brioschi Effervescent Antacid	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	6/5/2017	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Neobourne Pharma LP	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	69276-200	The 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 NAME	Brioschi Effervescent Antacid	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	9/23/2019	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Neobourne Pharma Lp	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

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