NDC Package 52605-022-10 Phentermine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
52605-022-10
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Phentermine Hydrochloride
Usage Information:
Phentermine hydrochloride tablets, USP  is indicated  as a short-term (a few weeks) adjunct in a regimen of weight reduction based on  exercise, behavioral modification and caloric restriction in the management of  exogenous obesity for patients with an initial body mass index ≥30 kg/m2,or ≥27 kg/m2 in the presence of other risk factors (e.g., controlled  hypertension, diabetes, hyperlipidemia).Below is a chart of body mass index (BMI) based on  various heights and weights. BMI is calculated by taking the patients weight, in kilograms (kg), divided by the patients height, in meters (m), squared. Metric conversions are as follows: pounds ÷ 2.2 = kg; inches x 0.0254 = meters.The limited usefulness of agents of this class, including  Phentermine hydrochloride tablets, USP [see Clinical Pharmacology (12.1, 12.2)] should be measured against  possible risk factors inherent in their use such as those described below.
11-Digit NDC Billing Format:
52605002210
NDC to RxNorm Crosswalk:
  • 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
  • Labeler Name:
    Polygen Pharmaceuticals Inc.
    Sample Package:
    No
    Start Marketing Date:
    11-18-2016
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    52605-022-01100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52605-022-10?

    The NDC Packaged Code 52605-022-10 is assigned to a package of 1000 tablet in 1 bottle of Phentermine Hydrochloride, labeled by Polygen Pharmaceuticals Inc.. The product's dosage form is and is administered via form.

    Is NDC 52605-022 included in the NDC Directory?

    No, Phentermine Hydrochloride with product code 52605-022 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Polygen Pharmaceuticals Inc. on November 18, 2016 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 52605-022-10?

    The 11-digit format is 52605002210. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-252605-022-105-4-252605-0022-10