0781-7157 NDC - IPRATROPIUM BROMIDE ()

Drug Information

Product NDC: 0781-7157

Proprietary Name: Ipratropium Bromide

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sandoz Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/1/2011

Package Information

No. Package Code Package Description Billing Unit
10781-7157-292 POUCH in 1 CARTON (0781-7157-29) / 30 AMPULE in 1 POUCH / 2.5 mL in 1 AMPULEML
20781-7157-641 POUCH in 1 CARTON (0781-7157-64) / 30 AMPULE in 1 POUCH / 2.5 mL in 1 AMPULEML
30781-7157-861 POUCH in 1 CARTON (0781-7157-86) / 25 AMPULE in 1 POUCH / 2.5 mL in 1 AMPULEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0781-7157The 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 NAMEIpratropium BromideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/1/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESandoz Inc.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