NDC 50383-740 Albuterol Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 50383-740?
What are the uses for Albuterol Sulfate?
Which are Albuterol Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALBUTEROL SULFATE (UNII: 021SEF3731)
- ALBUTEROL (UNII: QF8SVZ843E) (Active Moiety)
Which are 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- SACCHARIN (UNII: FST467XS7D)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Albuterol Sulfate?
- RxCUI: 755497 - albuterol sulfate 2 MG in 5 mL Oral Solution
- RxCUI: 755497 - albuterol 0.4 MG/ML Oral Solution
- RxCUI: 755497 - albuterol (as albuterol sulfate) 2 MG per 5 ML Syrup
- RxCUI: 755497 - albuterol 2 MG per 5 ML Syrup
* Please review the disclaimer below.
Patient Education
Albuterol
Albuterol is used to prevent and treat wheezing, difficulty breathing, chest tightness, and coughing caused by lung diseases such as asthma and chronic obstructive pulmonary disease (COPD; a group of diseases that affect the lungs and airways). Albuterol is in a class of medications called bronchodilators. It works by relaxing and opening the air passages to the lungs to make breathing easier.
[Learn More]
* Please review the disclaimer below.
[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".