Moxifloxacin NDC 72189-321

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-321Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0321Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
72189-321-05	72189032105	3 mL in 1 BOTTLE (72189-321-05)Marketed from Feb 7, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Moxifloxacin
Generic name (nonproprietary): moxifloxacin
Active ingredients: Moxifloxacin hydrochloride monohydrate — 5 mg/mL
Dosage form: Solution/ drops
Route: Ophthalmic
Labeler: Direct Rx
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202867
Marketing start: Feb 7, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Fluoroquinolones (Chemical structure)
Identifiers: Product ID 72189-321_2c3d2dfe-0fff-b986-e063-6294a90a84c9SPL ID 2c3d2dfe-0fff-b986-e063-6294a90a84c9SPL set ID d771e69b-7d9b-13fa-e053-2995a90ac161RxCUI 403818UNII B8956S8609
Pharmacologic class: Fluoroquinolone Antibacterial

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472189032105 followed by a unit qualifier and the quantity

Package 72189-0321-05. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 202867

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 202867
Product	Strength	Form · route	Labeler	Product NDC
Moxifloxacin	Moxifloxacin hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	A-S Medication Solutions	50090-6357
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Redpharm Drug	67296-2129
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Advanced Rx Pharmacy of Tennessee, LLC	80425-0379
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Lupin Pharmaceuticals, Inc.	68180-422