Diclofenac Sodium NDC 50090-2454

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-2454Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-2454Add 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
50090-2454-0	50090245400	1 BOTTLE, DROPPER in 1 CARTON (50090-2454-0) / 5 mL in 1 BOTTLE, DROPPERMarketed from Aug 12, 2016

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Diclofenac Sodium
Generic name (nonproprietary): diclofenac sodium
Active ingredients: Diclofenac sodium — 1 mg/mL
Dosage form: Solution/ drops
Route: Ophthalmic
Labeler: A-S Medication Solutions
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078792
Marketing start: Dec 28, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers: Product ID 50090-2454_98e8ede7-aa2f-4dfa-90de-b7a9c5b828b4SPL ID 98e8ede7-aa2f-4dfa-90de-b7a9c5b828b4SPL set ID 5d74488c-e092-415d-b19b-05318380d9b1RxCUI 854801UNII QTG126297Q
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

N450090245400 followed by a unit qualifier and the quantity

Package 50090-2454-00. 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 Jun 10, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Diclofenac sodium ophthalmic solution is indicated for the treatment of postoperative inflammation in patients who have undergone cataract extraction and for the temporary relief of pain and photophobia in patients undergoing corneal refractive surgery.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078792

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

FDA NDC Directory listings under ANDA 078792
Product	Strength	Form · route	Labeler	Product NDC
Diclofenac Sodium	Diclofenac sodium 1 mg/mL	Solution/ dropsOphthalmic	Bausch & Lomb Incorporated	24208-457