Diclofenac Sodium NDC 66267-071

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

NuCare Pharmaceuticals,Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077863

Marketing start

Aug 19, 2008

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 66267-071_2bae2a68-6eb9-5e6d-e063-6394a90aa6e5SPL ID 2bae2a68-6eb9-5e6d-e063-6394a90aa6e5SPL set ID 62edf474-9c16-d535-e053-2991aa0a4a09RxCUI 855926UNII QTG126297QUPC 0366267071147

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

N466267007114 followed by a unit qualifier and the quantity Copy

Package 66267-0071-14. 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 077863

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