Diclofenac Potassium NDC 72888-073

Product information

Brand name (proprietary)

Diclofenac Potassium

Generic name (nonproprietary)

diclofenac potassium

Active ingredients

Diclofenac potassium — 50 mg/1

Dosage form

Tablet, Coated

Route

Oral

Labeler

Advagen Pharma Ltd

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075229

Marketing start

Dec 19, 2020

Listing expires

Dec 31, 2027

Other FDA classes

Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)

Identifiers

Product ID 72888-073_5bfca526-a004-182e-e063-6394a90a2ffcSPL ID 5bfca526-a004-182e-e063-6394a90a2ffc

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

NDC on a medical claim

N472888007300 followed by a unit qualifier and the quantity Copy

Package 72888-0073-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 075229

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