NDC 68071-1737 Ipratropium Bromide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-1737 - Ipratropium Bromide
Product Packages
NDC Code 68071-1737-2
Package Description: 2.5 mL in 1 VIAL
Product Details
What is NDC 68071-1737?
What are the uses for Ipratropium Bromide?
Which are Ipratropium Bromide UNII Codes?
The UNII codes for the active ingredients in this product are:
- IPRATROPIUM BROMIDE (UNII: J697UZ2A9J)
- IPRATROPIUM (UNII: GR88G0I6UL) (Active Moiety)
Which are Ipratropium Bromide Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Ipratropium Bromide?
- RxCUI: 836358 - ipratropium bromide 0.02 % Inhalation Solution
- RxCUI: 836358 - ipratropium bromide 0.2 MG/ML Inhalation Solution
- RxCUI: 836358 - ipratropium bromide 0.5 MG per 2.5 ML Inhalation Solution
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Patient Education
Ipratropium Oral Inhalation
Ipratropium oral inhalation is used to prevent wheezing, shortness of breath, coughing, and chest tightness in people with chronic obstructive pulmonary disease (COPD; a group of diseases that affect the lungs and airways) such as chronic bronchitis (swelling of the air passages that lead to the lungs) and emphysema (damage to the air sacs in the lungs). Ipratropium is in a class of medications called bronchodilators. It works by relaxing and opening the air passages to the lungs to make breathing easier.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".