NDC 50090-3929 Naltrexone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3929 - Naltrexone Hydrochloride
Product Characteristics
Product Packages
NDC Code 50090-3929-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 50090-3929?
What are the uses for Naltrexone Hydrochloride?
Which are Naltrexone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- NALTREXONE HYDROCHLORIDE (UNII: Z6375YW9SF)
- NALTREXONE (UNII: 5S6W795CQM) (Active Moiety)
Which are Naltrexone Hydrochloride 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Naltrexone Hydrochloride?
- RxCUI: 1483744 - naltrexone HCl 50 MG Oral Tablet
- RxCUI: 1483744 - naltrexone hydrochloride 50 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Naltrexone
Naltrexone is used along with counseling and social support to help people who have stopped drinking alcohol and using street drugs continue to avoid drinking or using drugs. Naltrexone should not be used to treat people who are still using street drugs or drinking large amounts of alcohol. Naltrexone is in a class of medications called opiate antagonists. It works by decreasing the craving for alcohol and blocking the effects of opiate medications and opioid street drugs.
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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".