NDC 17478-291 Cromolyn Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-291 - Cromolyn Sodium
Product Packages
NDC Code 17478-291-11
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
Price per Unit: $0.55654 per ML
Product Details
What is NDC 17478-291?
What are the uses for Cromolyn Sodium?
Which are Cromolyn Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- CROMOLYN SODIUM (UNII: Q2WXR1I0PK)
- CROMOLYN (UNII: Y0TK0FS77W) (Active Moiety)
Which are Cromolyn Sodium 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:
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
What is the NDC to RxNorm Crosswalk for Cromolyn Sodium?
- RxCUI: 831109 - cromolyn sodium 4 % Ophthalmic Solution
- RxCUI: 831109 - cromolyn sodium 40 MG/ML Ophthalmic Solution
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Patient Education
Cromolyn Ophthalmic
Cromolyn ophthalmic is used to treat the symptoms of allergic conjunctivitis (a condition in which the eyes become itchy, swollen, red, and teary when they are exposed to certain substances) and keratitis (a condition that causes swelling of the cornea [tissue in the front of the eye] that causes eye redness, pain, and tearing and changes in vision) in adults and children 4 years of age and older. Cromolyn is in a class of medications called mast cell stabilizers. It works by preventing the release of substances that cause inflammation (swelling) of the eyes.
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* 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".