Moxifloxacin Ophthalmic Solution Solution/ Drops
NDC Package 67296-2222-3
Package Information
Moxifloxacin Ophthalmic Solution (moxifloxacin) solution/ dropses is moxifloxacin ophthalmic solution is indicated for the treatment of bacterial conjunctivitis caused by susceptible strains of the following organisms: Corynebacterium species*Micrococcus luteus*Staphylococcus aureusStaphylococcus epidermidisStaphylococcus haemolyticusStaphylococcus hominisStaphylococcus warneri*Streptococcus pneumoniaeStreptococcus viridansgroup Acinetobacter lwoffii*Haemophilus influenzaHaemophilus parainfluenzae*Chlamydia trachomatis*Efficacy for this organism was studied in fewer than 10 infections. This formulation utilizes a solution/ drops delivery system. Marketed by Redpharm Drug, this product is identified by NDC 67296-2222 and is authorized under FDA application ANDA217988.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 67296 - Redpharm Drug
- 67296-2222 - Moxifloxacin Ophthalmic Solution
- 67296-2222-3 - 1 BOTTLE in 1 CARTON / 3 mL in 1 BOTTLE
- 67296-2222 - Moxifloxacin Ophthalmic Solution
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.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 67296-2222-3 identifies a specific commercial package of 1 bottle in 1 carton / 3 ml in 1 bottle of Moxifloxacin Ophthalmic Solution, a human prescription drug labeled by Redpharm Drug. This solution/ drops is formulated for ophthalmic use and contains moxifloxacin hydrochloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Redpharm Drug on January 27, 2025. The current certification is valid through December 31, 2027.
How is this Redpharm Drug product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 67296222203. 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.