Phentermine Hydrochloride
NDC Package 61939-810-01
Package Information
Phentermine Hydrochloride is tablets are 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 patient’s weight, in kilograms (kg), divided by the patient’s height, in meters (m), squared. Marketed by Mikah Pharma, Llc, this product is identified by NDC 61939-810 and is authorized under FDA application ANDA040190.
Identification & Billing
- 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
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 61939 - Mikah Pharma, Llc
- 61939-810 - Phentermine Hydrochloride
- 61939-810-01 - 100 TABLET in 1 BOTTLE
- 61939-810 - Phentermine Hydrochloride
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 full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (61939-810). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 61939-810-01 identifies a specific commercial package of 100 tablet in 1 bottle of Phentermine Hydrochloride, labeled by Mikah Pharma, Llc. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Mikah Pharma, Llc on May 01, 2014. The current certification is valid through December 31, 2017.
How is this Mikah Pharma, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 61939081001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.