NDC codes

FDA NDC Directory
Product NDC (as listed)50090-4030Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-4030Add 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
50090-4030-0500904030001 TUBE in 1 CARTON (50090-4030-0) / 100 g in 1 TUBEMarketed from Jan 9, 2019

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 — 10 mg/g
Dosage form
Gel
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209903
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 50090-4030_007424b3-ecef-4ff0-8f86-90b1c2723290SPL ID 007424b3-ecef-4ff0-8f86-90b1c2723290SPL set ID 203f96bb-ae63-475c-b7a6-03c0dbc43597RxCUI 855633UNII QTG126297Q

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450090403000 followed by a unit qualifier and the quantity

Package 50090-4030-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Diclofenac sodium is a non-steroidal anti-inflammatory drug indicated for the relief of the pain of osteoarthritis of joints amenable to topical treatment, such as the knees and those of the hands. ( 1 ) Diclofenac sodium topical gel was not evaluated for use on joints of the spine, hip, or shoulder. ( 14.1 ) Diclofenac sodium topical gel is indicated for the relief of the pain of osteoarthritis of joints amenable to topical treatment, such as the knees and those of the hands. Diclofenac sodium topical gel has not been evaluated for use on the spine, hip, or shoulder.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209903

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

FDA NDC Directory listings under ANDA 209903
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalEXELAN PHARMACEUTICALS INC.76282-103
Diclofenac sodiumDiclofenac sodium 10 mg/gGelTopicalCipla USA Inc.69097-720
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalNuCare Pharmaceuticals, Inc.68071-3665
Diclofenac sodiumDiclofenac sodium 10 mg/gGelTopicalNuCare Pharmaceuticals, Inc.68071-5307
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalQuality Care Products, LLC83008-037
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalA-S Medication Solutions50090-4020

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