NDC 50090-4216 Phentermine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-4216 - Phentermine Hydrochloride
Product Characteristics
Product Packages
NDC Code 50090-4216-0
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-4216?
What are the uses for Phentermine Hydrochloride?
Which are Phentermine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENTERMINE HYDROCHLORIDE (UNII: 0K2I505OTV)
- PHENTERMINE (UNII: C045TQL4WP) (Active Moiety)
Which are Phentermine 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Phentermine Hydrochloride?
- RxCUI: 803353 - phentermine HCl 37.5 MG Oral Tablet
- RxCUI: 803353 - phentermine hydrochloride 37.5 MG Oral Tablet
- RxCUI: 803353 - phentermine hydrochloride 37.5 MG (equivalent to phentermine 30 MG) Oral Tablet
* Please review the disclaimer below.
Patient Education
Phentermine
Phentermine is used for a limited period of time to speed weight loss in overweight people who are exercising and eating a low-calorie diet. Phentermine is in a class of medications called anorectics. It works by decreasing appetite.
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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".