NDC codes

FDA NDC Directory
Product NDC (as listed)58602-606Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58602-0606Add 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
58602-606-21586020606211 KIT in 1 CARTON (58602-606-21) * 2 TUBE in 1 KIT / 150 g in 1 TUBE * 1 TUBE in 1 KIT / 50 g in 1 TUBEMarketed from May 10, 2023

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)
Diclofenac Sodium
Generic name (nonproprietary)
diclofenac sodium
Dosage form
Kit
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204306
Marketing start
Listing expires
Identifiers
Product ID 58602-606_aa7e21b9-c07f-48a6-9266-67a490fd2b8bSPL ID aa7e21b9-c07f-48a6-9266-67a490fd2b8bSPL set ID 81e964ff-6622-4054-bf01-6ed6eef6778fRxCUI 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N458602060621 followed by a unit qualifier and the quantity

Package 58602-0606-21. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 204306

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

FDA NDC Directory listings under ANDA 204306
ProductStrengthForm · routeLabelerProduct NDC
Amazon Basic Care Arthritis Paindiclofenac sodiumDiclofenac sodium 10 mg/gGelTopicalAmazon.com Services LLC72288-624
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalINNOVUS PHARMACEUTICALS, INC.57483-185
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalHarris Teeter72036-014
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurobindo Pharma Limited84386-120
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurohealth LLC58602-604
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurohealth LLC58602-609
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalKROGER COMPANY30142-277
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalRedpharm Drug67296-2155
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalSportpharm LLC85766-137
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalGERI-CARE PHARMACEUTICAL CORP57896-147
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-4135
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-4335

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