NDC codes

FDA NDC Directory
Product NDC (as listed)0065-0092Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00065-0092Add 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
0065-0092-650006500926512 VIAL in 1 CARTON (0065-0092-65) / 5 mL in 1 VIALMarketed from Sep 15, 1972

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Fluorescite
Generic name (nonproprietary)
fluorescein sodium
Active ingredients
Fluorescein sodium — 100 mg/mL
Dosage form
Injection, Solution
Route
Ophthalmic
Labeler
Alcon, Inc.NDC labeler code 0065
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021980
Marketing start
Listing expires
Other FDA classes
Dyes (Mechanism)
Identifiers
Product ID 0065-0092_b315434c-5397-4a9d-859e-ebd2a68ed2c3SPL ID b315434c-5397-4a9d-859e-ebd2a68ed2c3SPL set ID ebb3883c-71f6-4fd0-a7e6-0ba8e1136dd9UNII 93X55PE38X
Pharmacologic class
Diagnostic Dye

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

N400065009265 followed by a unit qualifier and the quantity

Package 00065-0092-65. 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)

FLUORESCITE ® Injection 10% is indicated in diagnostic fluorescein angiography or angioscopy of the retina and iris vasculature. FLUORESCITE ® Injection 10% is indicated in diagnostic fluorescein angiography or angioscopy of the retina and iris vasculature. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0065-0092

What is NDC 0065-0092?
0065-0092 is the product NDC for Fluorescite (fluorescein sodium), Fluorescein sodium 100 mg/mL injection, solution, listed with the FDA by Alcon, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Fluorescite (Fluorescein sodium).
What is the active ingredient?
Fluorescein sodium.
Who is the labeler?
Alcon, Inc., NDC labeler code 0065. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fluorescite?
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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