NDC 71152-201 Ipratropium Bromide And Albuterol Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71152 - Medical Supply Distribution, Llc.
- 71152-201 - Ipratropium Bromide And Albuterol Sulfate
Product Packages
NDC Code 71152-201-30
Package Description: 30 VIAL in 1 CARTON / 3 mL in 1 VIAL
NDC Code 71152-201-60
Package Description: 60 VIAL in 1 CARTON / 3 mL in 1 VIAL
Product Details
What is NDC 71152-201?
What are the uses for Ipratropium Bromide And Albuterol Sulfate?
Which are Ipratropium Bromide And Albuterol Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- IPRATROPIUM BROMIDE (UNII: J697UZ2A9J)
- IPRATROPIUM (UNII: GR88G0I6UL) (Active Moiety)
- ALBUTEROL SULFATE (UNII: 021SEF3731)
- ALBUTEROL (UNII: QF8SVZ843E) (Active Moiety)
Which are Ipratropium Bromide And Albuterol Sulfate 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Ipratropium Bromide And Albuterol Sulfate?
- RxCUI: 1437702 - ipratropium Br 0.5 MG / albuterol sulfate 3 MG in 3 ML Inhalation Solution
- RxCUI: 1437702 - albuterol 0.833 MG/ML / ipratropium bromide 0.167 MG/ML Inhalation Solution
- RxCUI: 1437702 - albuterol 2.5 MG (as albuterol sulfate 3 MG) / ipratropium bromide 0.5 MG per 3 ML Inhalation Solution
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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".