What is NDC 72162-2460?

72162-2460 is the product NDC for Divalproex Sodium, Divalproex sodium 250 mg/1 tablet, delayed release, listed with the FDA by Bryant Ranch Prepack. It has 3 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Divalproex Sodium?

188 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Divalproex Sodium NDC 72162-2460 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2460Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2460Add 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
72162-2460-1	7216224600172162246001	100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-1)Marketed from Feb 21, 2025
72162-2460-3	7216224600372162246003	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-3)Marketed from Feb 21, 2025
72162-2460-5	7216224600572162246005	500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-5)Marketed from Feb 21, 2025

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): Divalproex Sodium
Generic name (nonproprietary): divalproex sodium
Active ingredients: Divalproex sodium — 250 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 079163
Marketing start: Oct 1, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 72162-2460_92653b4d-75de-4377-9e7e-2b4527826d71SPL ID 92653b4d-75de-4377-9e7e-2b4527826d71SPL set ID 0fb57229-08ef-44d6-b40a-92b2f96ff795RxCUI 1099678UNII 644VL95AO6
Pharmacologic class: Anti-epileptic Agent; Mood Stabilizer

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

N472162246001 followed by a unit qualifier and the quantity

Package 72162-2460-01. 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

Current FDA label (SPL), effective Feb 21, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Divalproex sodium is an anti-epileptic drug indicated for: Treatment of manic episodes associated with bipolar disorder ( 1.1 ) Monotherapy and adjunctive therapy of complex partial seizures and simple and complex absence seizures; adjunctive therapy in patients with multiple seizure types that include absence seizures ( 1.2 ) Prophylaxis of migraine headaches ( 1.3 ) 1.1 Mania Divalproex sodium delayed-release tablets are valproate and is indicated for the treatment of the manic episodes associated with bipolar disorder. A manic episode is a distinct period of abnormally and persistently elevated, expansive, or irritable mood. Typical symptoms of mania include pressure of speech, motor hype…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2460

What is NDC 72162-2460?: 72162-2460 is the product NDC for Divalproex Sodium, Divalproex sodium 250 mg/1 tablet, delayed release, listed with the FDA by Bryant Ranch Prepack. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Divalproex Sodium.
What is the active ingredient?: Divalproex sodium.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Divalproex Sodium?: 188 other product NDCs are listed under this name. See all Divalproex 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 Divalproex Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Coupler LLC	67046-0875	67046-0875-03
divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	Coupler LLC	67046-1696	67046-1696-03
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Cardinal Health 107, LLC	55154-0577	55154-0577-00
divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-4193	68788-4193-0368788-4193-0668788-4193-09
divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Coupler LLC	67046-1683	67046-1683-03
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Unit Dose Solutions, Inc.	87441-027	87441-0027-01
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Unit Dose Solutions, Inc.	87441-028	87441-0028-01
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-2021	67046-2021-03
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-4100	68788-4100-0368788-4100-0668788-4100-09
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Safecor Health, LLC	48433-034	48433-0034-08

All 189 Divalproex Sodium NDCs

Other NDCs under ANDA 079163

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

FDA NDC Directory listings under ANDA 079163
Product	Strength	Form · route	Labeler	Product NDC
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-4575
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Coupler LLC	67046-0875
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-2626
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	71335-0008
Divalproex Sodium	Divalproex sodium 125 mg/1	Tablet, Delayed releaseOral	Unichem Pharmaceuticals (USA), Inc.	29300-138
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Unichem Pharmaceuticals (USA), Inc.	29300-139
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Unichem Pharmaceuticals (USA), Inc.	29300-140
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Northwind Health Company, LLC	51655-365
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Unit Dose Solutions, Inc.	87441-027
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Unit Dose Solutions, Inc.	87441-028
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-2007
Divalproex Sodium	Divalproex sodium 125 mg/1	Tablet, Delayed releaseOral	BluePoint Laboratories	68001-472
Divalproex Sodium	Divalproex sodium 125 mg/1	Tablet, Delayed releaseOral	American Health Packaging	60687-857
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	BluePoint Laboratories	68001-473
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	BluePoint Laboratories	68001-474
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	American Health Packaging	60687-868
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	63629-4278
Divalproex Sodium	Divalproex sodium 500 mg/1	Tablet, Delayed releaseOral	American Health Packaging	60687-879
Divalproex Sodium	Divalproex sodium 250 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	71335-2862
Divalproex Sodium	Divalproex sodium 125 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-4861

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