NDC 50436-6760 Phentermine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-6760 - Phentermine Hydrochloride
Product Characteristics
Product Packages
NDC Code 50436-6760-1
Package Description: 7 TABLET in 1 BOTTLE
NDC Code 50436-6760-2
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 50436-6760-3
Package Description: 21 TABLET in 1 BOTTLE
NDC Code 50436-6760-4
Package Description: 28 TABLET in 1 BOTTLE
Product Details
What is NDC 50436-6760?
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 (15 MPA.S AT 5%) (UNII: 68401960MK)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
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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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[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".