Minocycline Hydrochloride
NDC Package 53002-2210-4
Package Information
Minocycline Hydrochloride is capsules, USP are indicated in the treatment of the following infections due to susceptible strains of the designated microorganisms:Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox and tick fevers caused by rickettsiae.Respiratory tract infections caused by Mycoplasma pneumoniae.Lymphogranuloma venereum caused by Chlamydia trachomatis.Psittacosis (Ornithosis) due to Chlamydophila psittaci.Trachoma caused by Chlamydia trachomatis, although the infectious agent is not always eliminated, as judged by immunofluorescence.Inclusion conjunctivitis caused by Chlamydia trachomatis.Nongonococcal urethritis, endocervical, or rectal infections in adults caused by Ureaplasma urealyticum or Chlamydia trachomatis.Relapsing fever due to Borrelia recurrentis.Chancroid caused by Haemophilus ducreyi.Plague due to Yersinia pestis.Tularemia due to Francisella tularensis.Cholera caused by Vibrio cholerae.Campylobacter fetus infections caused by Campylobacter fetus.Brucellosis due to Brucella species (in conjunction with streptomycin). Marketed by Rpk Pharmaceuticals, Inc., this product is identified by NDC 53002-2210 and is authorized under FDA application ANDA065062.
Identification & Billing
- RxCUI: 197984 - minocycline HCl 100 MG Oral Capsule
- RxCUI: 197984 - minocycline 100 MG Oral Capsule
- RxCUI: 197984 - minocycline (as minocycline HCl) 100 MG Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 53002 - Rpk Pharmaceuticals, Inc.
- 53002-2210 - Minocycline Hydrochloride
- 53002-2210-4 - 14 CAPSULE in 1 BOTTLE
- 53002-2210 - Minocycline 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.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (53002-2210). 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 53002-2210-4 identifies a specific commercial package of 14 capsule in 1 bottle of Minocycline Hydrochloride, labeled by Rpk Pharmaceuticals, Inc.. 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 Rpk Pharmaceuticals, Inc. on April 02, 2015. The current certification is valid through December 31, 2024.
How is this Rpk Pharmaceuticals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 53002221004. 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 Package segment to maintain the 5-4-2 structure.