Moxifloxacin Hydrochloride NDC 71335-2815

Product information

Brand name (proprietary)

Moxifloxacin Hydrochloride

Generic name (nonproprietary)

moxifloxacin hydrochloride

Active ingredients

Moxifloxacin hydrochloride — 400 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 202632

Marketing start

Mar 4, 2014

Listing expires

Dec 31, 2026

Other FDA classes

Fluoroquinolones (Chemical structure)

Identifiers

Product ID 71335-2815_6ac508d3-c5c6-49b1-ab21-56896601f8adSPL ID 6ac508d3-c5c6-49b1-ab21-56896601f8adSPL set ID ac8a81b9-2fed-412a-8c83-db8dee1061f6RxCUI 311787UNII C53598599T

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335281501 followed by a unit qualifier and the quantity Copy

Package 71335-2815-01. 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 202632

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