Diclofenac Sodium Delayed Release NDC 63187-222

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-222Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0222Add 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 NDC	11-digit (billing)	Package
63187-222-15	63187022215	15 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-222-15)Marketed from Sep 1, 2014
63187-222-30	63187022230	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-222-30)Marketed from Sep 1, 2014
63187-222-60	63187022260	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-222-60)Marketed from Sep 1, 2014
63187-222-90	63187022290	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-222-90)Marketed from Sep 1, 2014

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 Delayed ReleaseSuffix: Delayed Release
Generic name (nonproprietary): diclofenac sodium
Active ingredients: Diclofenac sodium — 75 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: Proficient Rx LP
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075185
Marketing start: Nov 13, 1998
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers: Product ID 63187-222_108a4ddb-0e11-472d-989a-5617e8823008SPL ID 108a4ddb-0e11-472d-989a-5617e8823008SPL set ID 73a46413-ecbc-4453-814d-bec955b375d2RxCUI 855926UNII QTG126297QUPC 0363187222604
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

N463187022215 followed by a unit qualifier and the quantity

Package 63187-0222-15. 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

Current FDA label (SPL), effective Feb 1, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential bene ts and risks of diclofenac sodium delayed-release tablets and other treatment options before deciding to use diclofenac. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Diclofenac is indicated: • For relief of the signs and symptoms of osteoarthritis • For relief of the signs and symptoms of rheumatoid arthritis • For acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 075185

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

FDA NDC Directory listings under ANDA 075185
Product	Strength	Form · route	Labeler	Product NDC
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-0756
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-967
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-968
Diclofenac Sodium DRdiclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0189
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-0542
Diclofenac Sodium DRdiclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0197
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-0543
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-0545
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	71335-0357
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-0627
Diclofenac Sodium D/R	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	DirectRx	72189-675
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	Carlsbad Technology, Inc.	61442-102
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 25 mg/1	Tablet, Delayed releaseOral	Carlsbad Technology, Inc.	61442-101
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Carlsbad Technology, Inc.	61442-103
Diclofenac Sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	AvKARE	42291-231
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	NuCare Pharmaceuticals, Inc.	68071-3184
Diclofenac Sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	AvKARE	42291-230
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	PHOENIX RX LLC	85509-1103
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	Carlsbad Technology, Inc.	61442-226
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Carlsbad Technology, Inc.	61442-227

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