Diclofenac Sodium Delayed Release (Diclofenac sodium) NDC 68788-8952

Product information

Brand name (proprietary)

Diclofenac Sodium Delayed ReleaseSuffix: Delayed Release

Generic name (nonproprietary)

diclofenac sodium

Active ingredients

Diclofenac sodium — 50 mg/1

Dosage form

Tablet, Delayed release

Route

Oral

Labeler

Preferred Pharmaceuticals Inc.NDC labeler code 68788

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075185

Marketing start

Nov 20, 2015

Listing expires

Dec 31, 2027

Other FDA classes

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

Identifiers

Product ID 68788-8952_274d233d-803b-4a98-9d5b-da925f2e5147SPL ID 274d233d-803b-4a98-9d5b-da925f2e5147SPL set ID e947653c-6789-4c15-82c9-4b1402f6d6acRxCUI 855906UNII 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

N468788895201 followed by a unit qualifier and the quantity Copy

Package 68788-8952-01. 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

About NDC 68788-8952

What is NDC 68788-8952?

68788-8952 is the product NDC for Diclofenac Sodium Delayed Release, Diclofenac sodium 50 mg/1 tablet, delayed release, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Diclofenac Sodium Delayed Release (Diclofenac Sodium).

What is the active ingredient?

Diclofenac sodium.

Who is the labeler?

Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Diclofenac Sodium Delayed Release?

47 other product NDCs are listed under this name. See all Diclofenac Sodium Delayed Release NDCs.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory. See Billing references above.

Related NDCs: other Diclofenac Sodium Delayed Release products

Other finished products listed under the same name: strengths, forms and labelers.

All 48 Diclofenac Sodium Delayed Release NDCs

Other NDCs under ANDA 075185

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

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