NDC codes

FDA NDC Directory
Product NDC (as listed)70518-2811Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-2811Add 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
70518-2811-070518281100705182811001 BOTTLE, DROPPER in 1 CARTON (70518-2811-0) / 150 mL in 1 BOTTLE, DROPPERMarketed from Jul 10, 2020

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 — 16.05 mg/mL
Dosage form
Solution
Route
Topical
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203818
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 70518-2811_4e42d4e0-b229-84ef-e063-6294a90ab3cbSPL ID 4e42d4e0-b229-84ef-e063-6294a90ab3cbSPL set ID d349d286-b462-4f8f-aa39-6173653175d6RxCUI 857700UNII 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

N470518281100 followed by a unit qualifier and the quantity

Package 70518-2811-00. 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 topical solution, USP is indicated for the treatment of signs and symptoms of osteoarthritis of the knee(s) (1). Diclofenac sodium topical solution is a nonsteroidal anti-inflammatory drug indicated for the treatment of signs and symptoms of osteoarthritis of the knee(s). ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-2811

What is NDC 70518-2811?
70518-2811 is the product NDC for Diclofenac Sodium, Diclofenac sodium 16.05 mg/mL solution, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Diclofenac Sodium.
What is the active ingredient?
Diclofenac sodium.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diclofenac Sodium?
241 other product NDCs are listed under this name. See all Diclofenac 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 Diclofenac Sodium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Diclofenac Sodiumdiclofenac sodium topical gel, 1%Diclofenac sodium 10 mg/gGelTopicalIPG Pharmaceuticals, inc.71085-08471085-0084-03
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalTarget Corporation11673-02811673-0028-1011673-0028-15
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralNorthwind Health Company, LLC82868-11482868-0114-30
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-413568788-4135-01
Diclofenac SodiumDiclofenac sodium 100 mg/1Tablet, Film coated, Extended releaseOralAurobindo Pharma Limited84386-10384386-0103-01
Diclofenac SodiumDiclofenac sodium 50 mg/1Tablet, Delayed releaseOralREMEDYREPACK INC.70518-469470518-4694-00
Diclofenac sodiumDiclofenac sodium 30 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-411868788-4118-01
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-433568788-4335-01
Diclofenac SodiumDiclofenac sodium 25 mg/1Tablet, Delayed releaseOralUmedica Laboratories USA Inc.60290-08260290-0082-01
Diclofenac SodiumDiclofenac sodium 50 mg/1Tablet, Delayed releaseOralUmedica Laboratories USA Inc.60290-08360290-0083-0160290-0083-0260290-0083-03+1 more

All 242 Diclofenac Sodium NDCs

Other NDCs under ANDA 203818

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

FDA NDC Directory listings under ANDA 203818
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalA-S Medication Solutions50090-6713
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalSun Pharmaceutical Industries, Inc.51672-1358
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalPreferred Pharmaceuticals, Inc.68788-7715
Diclofenac sodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalProficient Rx LP71205-062
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalProficient Rx LP71205-579
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalDirectRx72189-319
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalDirect_Rx72189-454
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalAsclemed USA, Inc.76420-919
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalAdvanced Rx of Tennessee, LLC80425-0361

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