NDC codes

FDA NDC Directory
Product NDC (as listed)82667-700Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82667-0700Add 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 NDC11-digit (billing)PackageCopy
82667-700-0382667070003826670700031 BOTTLE in 1 CARTON (82667-700-03) / 3 mL in 1 BOTTLEMarketed from Jul 1, 2024

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)
Vigamox
Generic name (nonproprietary)
moxifloxacin hydrochloride
Active ingredients
Moxifloxacin hydrochloride — 5 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
Harrow Eye, LLCNDC labeler code 82667
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021598
Marketing start
Listing expires
Other FDA classes
Fluoroquinolones (Chemical structure)
Identifiers
Product ID 82667-700_48fbfef1-1e3b-4558-e063-6394a90a2454SPL ID 48fbfef1-1e3b-4558-e063-6394a90a2454SPL set ID 12053b08-7e66-c6f3-e063-6394a90a9cd9RxCUI 403818, 404473UNII C53598599T

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

N482667070003 followed by a unit qualifier and the quantity

Package 82667-0700-03. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

VIGAMOX ® is indicated for the treatment of bacterial conjunctivitis caused by susceptible strains of the following organisms: Corynebacterium species* Micrococcus luteus* Staphylococcus aureus Staphylococcus epidermidis Staphylococcus haemolyticus Staphylococcus hominis Staphylococcus warneri* Streptococcus pneumoniae Streptococcus viridans group Acinetobacter lwoffii* Haemophilus influenza Haemophilus parainfluenzae* Chlamydia trachomatis *Efficacy for this organism was studied in fewer than 10 infections. VIGAMOX is a topical fluoroquinolone anti-infective indicated for the treatment of bacterial conjunctivitis caused by susceptible strains of the following organisms: Corynebacterium spec…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82667-700

What is NDC 82667-700?
82667-700 is the product NDC for Vigamox (moxifloxacin hydrochloride), Moxifloxacin hydrochloride 5 mg/mL solution/ drops, listed with the FDA by Harrow Eye, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Vigamox (Moxifloxacin hydrochloride).
What is the active ingredient?
Moxifloxacin hydrochloride.
Who is the labeler?
Harrow Eye, LLC, NDC labeler code 82667. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Vigamox?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under NDA 021598

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

FDA NDC Directory listings under NDA 021598
ProductStrengthForm · routeLabelerProduct NDC
Moxifloxacin Ophthalmic Solutionmoxifloxacin hydrochlorideMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicSandoz Inc0781-7135

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