What is NDC 69292-722?

69292-722 is the product NDC for Flurbiprofen Sodium, Flurbiprofen sodium .3 mg/mL solution/ drops, listed with the FDA by Amici Pharma, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Amici Pharma, Inc., NDC labeler code 69292. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Flurbiprofen Sodium?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Flurbiprofen Sodium NDC 69292-722 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69292-722Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69292-0722Add 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
69292-722-25	6929207222569292072225	1 BOTTLE, DROPPER in 1 CARTON (69292-722-25) / 2.5 mL in 1 BOTTLE, DROPPERMarketed from Mar 31, 2018

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): Flurbiprofen Sodium
Generic name (nonproprietary): flurbiprofen sodium
Active ingredients: Flurbiprofen sodium — .3 mg/mL
Dosage form: Solution/ drops
Route: Ophthalmic
Labeler: Amici Pharma, Inc.NDC labeler code 69292
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074447
Marketing start: Mar 31, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 69292-722_1ec17137-cc34-44e9-b03f-efcafeb0fe05SPL ID 1ec17137-cc34-44e9-b03f-efcafeb0fe05SPL set ID c27f2d57-4b9d-4b78-8d85-3bac84f733b1RxCUI 1243585UNII Z5B97MU9K4
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N469292072225 followed by a unit qualifier and the quantity

Package 69292-0722-25. 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 Apr 14, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Flurbiprofen sodium ophthalmic solution is indicated for the inhibition of intraoperative miosis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69292-722

What is NDC 69292-722?: 69292-722 is the product NDC for Flurbiprofen Sodium, Flurbiprofen sodium .3 mg/mL solution/ drops, listed with the FDA by Amici Pharma, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Flurbiprofen Sodium.
What is the active ingredient?: Flurbiprofen sodium.
Who is the labeler?: Amici Pharma, Inc., NDC labeler code 69292. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Flurbiprofen Sodium?: 3 other product NDCs are listed under this name. See all Flurbiprofen Sodium NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Flurbiprofen Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Flurbiprofen Sodium	Flurbiprofen sodium .3 mg/mL	Solution/ dropsOphthalmic	A-S Medication Solutions	50090-3946	50090-3946-00
Flurbiprofen Sodium	Flurbiprofen sodium .3 mg/mL	Solution/ dropsOphthalmic	Bausch & Lomb Incorporated	24208-314	24208-0314-25
Flurbiprofen Sodium	Flurbiprofen sodium .3 mg/mL	Solution/ dropsOphthalmic	Proficient Rx LP	63187-937	63187-0937-25

Other NDCs under ANDA 074447

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

FDA NDC Directory listings under ANDA 074447
Product	Strength	Form · route	Labeler	Product NDC
Flurbiprofen Sodium	Flurbiprofen sodium .3 mg/mL	Solution/ dropsOphthalmic	Bausch & Lomb Incorporated	24208-314
Flurbiprofen Sodium	Flurbiprofen sodium .3 mg/mL	Solution/ dropsOphthalmic	A-S Medication Solutions	50090-3946
Flurbiprofen Sodium	Flurbiprofen sodium .3 mg/mL	Solution/ dropsOphthalmic	Proficient Rx LP	63187-937