Diclofenac Sodium NDC 71335-2684

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

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 216548

Marketing start

May 11, 2023

Listing expires

Dec 31, 2027

Other FDA classes

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

Identifiers

Product ID 71335-2684_a18f3fb9-d435-4b8f-9081-22d615fe35ebSPL ID a18f3fb9-d435-4b8f-9081-22d615fe35ebSPL set ID 03c4f06f-6a49-4404-bf3b-0aafa33c81efRxCUI 855926UNII QTG126297Q

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

N471335268400 followed by a unit qualifier and the quantity Copy

Package 71335-2684-00. 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.