NDC codes

FDA NDC Directory
Product NDC (as listed)82667-600Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82667-0600Add 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
82667-600-0582667060005826670600051 BOTTLE, PLASTIC in 1 CARTON (82667-600-05) / 5 mL in 1 BOTTLE, PLASTICMarketed from Apr 7, 2025

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)
Maxidex
Generic name (nonproprietary)
dexamethasone
Active ingredients
Dexamethasone — 1 mg/mL
Dosage form
For suspension
Route
Ophthalmic
Labeler
Harrow Eye, LLCNDC labeler code 82667
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 013422
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 82667-600_34661206-e37a-6ce7-e063-6394a90aaf85SPL ID 34661206-e37a-6ce7-e063-6394a90aaf85SPL set ID 35e47fcd-e020-43e5-8322-41f8060d220dRxCUI 205669, 309692UNII 7S5I7G3JQLUPC 0382667600053
Pharmacologic class
Corticosteroid

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

N482667060005 followed by a unit qualifier and the quantity

Package 82667-0600-05. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe, such as allergic conjunctivitis, acne rosacea, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, selected infective conjunctivitides when the inherent hazard of steroid use is accepted to obtain an advisable diminution in edema and inflammation; corneal injury from chemical, radiation, or thermal burns, or penetration of foreign bodies.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82667-600

What is NDC 82667-600?
82667-600 is the product NDC for Maxidex (dexamethasone), Dexamethasone 1 mg/mL for suspension, 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?
Maxidex (Dexamethasone).
What is the active ingredient?
Dexamethasone.
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 Maxidex?
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.

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