NDC Package 12634-687-67 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:
12634-687-67
Package Description:
7 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Phentermine Hydrochloride
Usage Information:
Phentermine hydrochloride 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/m 2, or ≥ 27 kg/m 2 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 patient's weight, in kilograms (kg), divided by the patient's height, in meters (m), squared. Metric conversions are as follows:pounds ÷ 2.2 = kg; inches × 0.0254 = meters.BODY MASS INDEX (BMI), kg/m 2The limited usefulness of agents of this class, including phentermine hydrochloride tablets, [ 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:
12634068767
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:
    Apotheca Inc.
    Sample Package:
    No
    Start Marketing Date:
    10-23-2003
    Listing Expiration Date:
    12-31-2019
    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
    12634-687-0010 TABLET in 1 BOTTLE
    12634-687-01100 TABLET in 1 BOTTLE
    12634-687-0935 TABLET in 1 BOTTLE
    12634-687-4040 TABLET in 1 BOTTLE
    12634-687-4242 TABLET in 1 BOTTLE
    12634-687-4545 TABLET in 1 BOTTLE
    12634-687-5050 TABLET in 1 BOTTLE
    12634-687-5212 TABLET in 1 BLISTER PACK
    12634-687-5414 TABLET in 1 BLISTER PACK
    12634-687-5720 TABLET in 1 BLISTER PACK
    12634-687-5828 TABLET in 1 BLISTER PACK
    12634-687-5930 TABLET in 1 BLISTER PACK
    12634-687-6060 TABLET in 1 BOTTLE
    12634-687-6110 TABLET in 1 BLISTER PACK
    12634-687-633 TABLET in 1 BLISTER PACK
    12634-687-666 TABLET in 1 BLISTER PACK
    12634-687-699 TABLET in 1 BLISTER PACK
    12634-687-7130 TABLET in 1 BOTTLE
    12634-687-7424 TABLET in 1 BOTTLE
    12634-687-7828 TABLET in 1 BOTTLE
    12634-687-7925 TABLET in 1 BOTTLE
    12634-687-8020 TABLET in 1 BOTTLE
    12634-687-8121 TABLET in 1 BOTTLE
    12634-687-8212 TABLET in 1 BOTTLE
    12634-687-8414 TABLET in 1 BOTTLE
    12634-687-8515 TABLET in 1 BOTTLE
    12634-687-9090 TABLET in 1 BOTTLE
    12634-687-911 TABLET in 1 BLISTER PACK
    12634-687-922 TABLET in 1 BOTTLE
    12634-687-933 TABLET in 1 BOTTLE
    12634-687-944 TABLET in 1 BOTTLE
    12634-687-955 TABLET in 1 BOTTLE
    12634-687-966 TABLET in 1 BOTTLE
    12634-687-977 TABLET in 1 BOTTLE
    12634-687-988 TABLET in 1 BOTTLE
    12634-687-999 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 12634-687-67?

    The NDC Packaged Code 12634-687-67 is assigned to a package of 7 tablet in 1 blister pack of Phentermine Hydrochloride, labeled by Apotheca Inc.. The product's dosage form is and is administered via form.

    Is NDC 12634-687 included in the NDC Directory?

    No, Phentermine Hydrochloride with product code 12634-687 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Apotheca Inc. on October 23, 2003 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 12634-687-67?

    The 11-digit format is 12634068767. 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
    5-3-212634-687-675-4-212634-0687-67