NDC 55700-383 Movantik
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 55700-383?
What are the uses for Movantik?
Which are Movantik UNII Codes?
The UNII codes for the active ingredients in this product are:
- NALOXEGOL OXALATE (UNII: 65I14TNM33)
- NALOXEGOL (UNII: 44T7335BKE) (Active Moiety)
Which are Movantik 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:
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Movantik?
- RxCUI: 1551782 - naloxegol 25 MG Oral Tablet
- RxCUI: 1551782 - naloxegol 25 MG (as naloxegol oxalate 28.5 MG) Oral Tablet
- RxCUI: 1601373 - movantik 25 MG Oral Tablet
- RxCUI: 1601373 - naloxegol 25 MG Oral Tablet [Movantik]
- RxCUI: 1601373 - Movantik 25 MG (as naloxegol oxalate 28.5 MG) Oral Tablet
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Patient Education
Naloxegol
Naloxegol is used to treat constipation caused by opiate (narcotic) pain medications in adults with chronic (ongoing) pain that is not caused by cancer. Naloxegol is in a class of medications called peripherally acting mu-opioid receptor antagonists. It works by protecting the bowel from the effects of opiate (narcotic) medications.
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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".