NDC 53217-172 Phentermine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53217 - Aidarex Pharmaceuticals Llc
- 53217-172 - Phentermine Hydrochloride
Product Characteristics
Product Packages
NDC Code 53217-172-07
Package Description: 7 TABLET in 1 BOTTLE
NDC Code 53217-172-14
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 53217-172-15
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 53217-172-21
Package Description: 21 TABLET in 1 BOTTLE
NDC Code 53217-172-28
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 53217-172-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 53217-172-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 53217-172-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 53217-172-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 53217-172-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 53217-172?
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:
- CROSPOVIDONE (UNII: 2S7830E561)
- CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
* 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".