NDC 50436-0101 Phentermine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-0101 - Phentermine Hydrochloride
Product Characteristics
Product Packages
NDC Code 50436-0101-1
Package Description: 7 TABLET in 1 BOTTLE
NDC Code 50436-0101-2
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 50436-0101-3
Package Description: 21 TABLET in 1 BOTTLE
NDC Code 50436-0101-4
Package Description: 28 TABLET in 1 BOTTLE
Product Details
What is NDC 50436-0101?
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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
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.
[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".