NDC 50090-0326 Diethylpropion Hcl Immediate-release

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50090-0326
Proprietary Name:
Diethylpropion Hcl Immediate-release
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A-s Medication Solutions
Labeler Code:
50090
Start Marketing Date: [9]
08-06-1959
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
ROUND (C48348)
Size(s):
19 MM
10 MM
Imprint(s):
WATSON;782
WATSON;783
Score:
1

Product Packages

NDC Code 50090-0326-3

Package Description: 14 TABLET in 1 BOTTLE

NDC Code 50090-0326-4

Package Description: 28 TABLET in 1 BOTTLE

NDC Code 50090-0326-5

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 50090-0326-7

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 50090-0326-8

Package Description: 30 TABLET in 1 BOTTLE

Product Details

What is NDC 50090-0326?

The NDC code 50090-0326 is assigned by the FDA to the product Diethylpropion Hcl Immediate-release which is product labeled by A-s Medication Solutions. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 50090-0326-3 14 tablet in 1 bottle , 50090-0326-4 28 tablet in 1 bottle , 50090-0326-5 90 tablet in 1 bottle , 50090-0326-7 60 tablet in 1 bottle , 50090-0326-8 30 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Diethylpropion Hcl Immediate-release?

Diethylpropion hydrochloride is indicated in the management of exogenous obesity as a short-term adjunct (a few weeks) in a regimen of weight reduction based on caloric restriction in patients with an initial body mass index (BMI) of 30 kg/m2 or higher and who have not responded to appropriate weight reducing regimen (diet and/or exercise) alone. Below is a chart of BMI based on various heights and weights. BMI is calculated by taking the patient’s weight, in kilograms (kg), divided by the patient’s height, in meters (m), squared. Metric conversions are as follows: pounds divided by 2.2 = kg; inches x 0.0254 = meters.Body Mass Index (BMI), kg/m2 Weight (pounds) Height (feet, inches)  5’0” 5’3” 5’6” 5’9” 6’0” 6’3” 140 27 25 23 21 19 18 150 29 27 24 22 20 19 160 31 28 26 24 22 20 170 33 30 28 25 23 21 180 35 32 29 27 25 23 190 37 34 31 28 26 24 200 39 36 32 30 27 25 210 41 37 34 31 29 26 220 43 39 36 33 30 28 230 45 41 37 34 31 29 240 47 43 39 36 33 30 250 49 44 40 37 34 31The usefulness of agents of this class (see CLINICAL PHARMACOLOGY) should be measured against possible risk factors inherent in their use such as those described below. Diethylpropion hydrochloride is indicated for use as monotherapy only.

Which are Diethylpropion Hcl Immediate-release UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Diethylpropion Hcl Immediate-release 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:

What is the NDC to RxNorm Crosswalk for Diethylpropion Hcl Immediate-release?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 978654 - diethylpropion HCl 25 MG Oral Tablet
  • RxCUI: 978654 - diethylpropion hydrochloride 25 MG Oral Tablet
  • RxCUI: 978668 - diethylpropion HCl 75 MG 24HR Extended Release Oral Tablet
  • RxCUI: 978668 - 24 HR diethylpropion hydrochloride 75 MG Extended Release Oral Tablet
  • RxCUI: 978668 - diethylpropion hydrochloride 75 MG 24 HR Extended Release Oral Tablet

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Product Footnotes

[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".