Prescription drug · ANDA

Diclofenac Sodium NDC 50090-7647

Diclofenac sodium 75 mg/1 · Tablet, Delayed release · Oral · A-S Medication Solutions

NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7647Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7647Add 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
50090-7647-05009076470090 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7647-0)Marketed from Sep 3, 2025

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 — 75 mg/1
Dosage form
Tablet, Delayed release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216548
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 50090-7647_6b9a6a44-9dd6-44a3-a9dd-037469d78110SPL ID 6b9a6a44-9dd6-44a3-a9dd-037469d78110SPL set ID 4c5b722e-0d1a-48e9-87c8-9b370b8ced46RxCUI 855926UNII 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450090764700 followed by a unit qualifier and the quantity

Package 50090-7647-00. 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

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

Other NDCs under ANDA 216548

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

FDA NDC Directory listings under ANDA 216548
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralA-S Medication Solutions50090-7646
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralRedpharm Drug67296-2151
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralBryant Ranch Prepack71335-2684
Diclofenac SodiumDiclofenac sodium 25 mg/1Tablet, Delayed releaseOralAdvagen Pharma Ltd72888-109
Diclofenac SodiumDiclofenac sodium 50 mg/1Tablet, Delayed releaseOralAdvagen Pharma Ltd72888-110
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralAdvagen Pharma Ltd72888-111
Diclofenac SodiumDiclofenac sodium 25 mg/1Tablet, Delayed releaseOralNorthStar Rx LLC72603-600
Diclofenac SodiumDiclofenac sodium 50 mg/1Tablet, Delayed releaseOralNorthStar Rx LLC72603-601
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralNorthStar Rx LLC72603-604

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