What is NDC 67296-1197?

67296-1197 is the product NDC for Diclofenac Sodium, Diclofenac sodium 75 mg/1 tablet, delayed release, listed with the FDA by RedPharm Drug, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

RedPharm Drug, Inc., NDC labeler code 67296. 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?

241 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Diclofenac Sodium NDC 67296-1197 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67296-1197Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67296-1197Add 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
67296-1197-2	6729611970267296119702	20 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-2)Marketed from Nov 13, 1998
67296-1197-3	6729611970367296119703	30 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-3)Marketed from Nov 13, 1998
67296-1197-6	6729611970667296119706	60 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-6)Marketed from Nov 13, 1998

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Generic name (nonproprietary): diclofenac sodium
Active ingredients: Diclofenac sodium — 75 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: RedPharm Drug, Inc.NDC labeler code 67296
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 67296-1197_3252d443-e09c-9209-e063-6294a90a5b2eSPL ID 3252d443-e09c-9209-e063-6294a90a5b2eSPL set ID 4ecb7bdc-4a5e-7444-e054-00144ff88e88RxCUI 855926UNII QTG126297QUPC 0367296119725
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

N467296119702 followed by a unit qualifier and the quantity

Package 67296-1197-02. 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 Apr 9, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits 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 the signs and symptoms of ankylosing spondylitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67296-1197

What is NDC 67296-1197?: 67296-1197 is the product NDC for Diclofenac Sodium, Diclofenac sodium 75 mg/1 tablet, delayed release, listed with the FDA by RedPharm Drug, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Diclofenac Sodium.
What is the active ingredient?: Diclofenac sodium.
Who is the labeler?: RedPharm Drug, Inc., NDC labeler code 67296. 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?: 241 other product NDCs are listed under this name. See all Diclofenac Sodium NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

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

Other Diclofenac Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Diclofenac Sodiumdiclofenac sodium topical gel, 1%	Diclofenac sodium 10 mg/g	GelTopical	IPG Pharmaceuticals, inc.	71085-084	71085-0084-03
Diclofenac Sodium	Diclofenac sodium 10 mg/g	GelTopical	Target Corporation	11673-028	11673-0028-1011673-0028-15
Diclofenac Sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Northwind Health Company, LLC	82868-114	82868-0114-30
Diclofenac Sodium	Diclofenac sodium 10 mg/g	GelTopical	Preferred Pharmaceuticals Inc.	68788-4135	68788-4135-01
Diclofenac Sodium	Diclofenac sodium 100 mg/1	Tablet, Film coated, Extended releaseOral	Aurobindo Pharma Limited	84386-103	84386-0103-01
Diclofenac Sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-4694	70518-4694-00
Diclofenac sodium	Diclofenac sodium 30 mg/g	GelTopical	Preferred Pharmaceuticals Inc.	68788-4118	68788-4118-01
Diclofenac Sodium	Diclofenac sodium 10 mg/g	GelTopical	Preferred Pharmaceuticals Inc.	68788-4335	68788-4335-01
Diclofenac Sodium	Diclofenac sodium 25 mg/1	Tablet, Delayed releaseOral	Umedica Laboratories USA Inc.	60290-082	60290-0082-01
Diclofenac Sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	Umedica Laboratories USA Inc.	60290-083	60290-0083-0160290-0083-0260290-0083-03+1 more

All 242 Diclofenac Sodium NDCs

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	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	AvKARE	42291-230
Diclofenac Sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	AvKARE	42291-231
Diclofenac Sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	SOLA Pharmaceuticals, LLC	70512-784
Diclofenac Sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0564
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	A-S Medication Solutions	50090-0542
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	A-S Medication Solutions	50090-7818
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-7838
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-7839
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-7880
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-7881
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 25 mg/1	Tablet, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-536
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-537
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-538
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 Delayed Releasediclofenac sodium	Diclofenac sodium 75 mg/1	Tablet, Delayed releaseOral	Northwind Health Company, LLC	51655-176
Diclofenac Sodium Delayed Releasediclofenac sodium	Diclofenac sodium 50 mg/1	Tablet, Delayed releaseOral	Northwind Health Company, LLC	51655-280

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