1. Home
  2. Labeler Index
  3. Pd-rx Pharmaceuticals, Inc.
  4. 72789-529
  5. NDC Package Code: 72789-529-30 Minocycline Hydrochloride

NDC Package 72789-529-30 Minocycline Hydrochloride

Tablet, Film Coated, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
72789-529-30
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
72789-529
Proprietary Name:
Minocycline Hydrochloride
Non-Proprietary Name:
Minocycline Hydrochloride
Substance Name:
Minocycline Hydrochloride
Usage Information:
This drug is contraindicated in persons who have shown hypersensitivity to any of the tetracyclines.
11-Digit NDC Billing Format:
72789052930
Product Type:
Human Prescription Drug
Labeler Name:
Pd-rx Pharmaceuticals, Inc.
Dosage Form:
Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
MINOCYCLINE HYDROCHLORIDE 115 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA204453
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-30-2016
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
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.

Frequently Asked Questions

What is NDC 72789-529-30?

The NDC Packaged Code 72789-529-30 is assigned to a package of 30 tablet, film coated, extended release in 1 bottle, plastic of Minocycline Hydrochloride, a human prescription drug labeled by Pd-rx Pharmaceuticals, Inc.. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

Is NDC 72789-529 included in the NDC Directory?

Yes, Minocycline Hydrochloride with product code 72789-529 is active and included in the NDC Directory. The product was first marketed by Pd-rx Pharmaceuticals, Inc. on September 30, 2016 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72789-529-30?

The 11-digit format is 72789052930. 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
5-3-272789-529-305-4-272789-0529-30