Divalproex sodium NDC 70518-1897

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-1897Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-1897Add 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	Copy
70518-1897-0	70518189700	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-1897-0)Marketed from Feb 22, 2019
70518-1897-1	70518189701	100 POUCH in 1 BOX (70518-1897-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1897-2)Marketed from Feb 22, 2019

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 — 500 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202419
Marketing start: Feb 22, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 70518-1897_593d6419-40ab-cfe7-e063-6294a90ae7a4SPL ID 593d6419-40ab-cfe7-e063-6294a90ae7a4SPL set ID 66b0a3e0-70df-469e-845f-17769482304bRxCUI 1099569UNII 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

N470518189700 followed by a unit qualifier and the quantity

Package 70518-1897-00. 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 Aug 17, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Divalproex sodium extended-release tablets are indicated for: Acute treatment of manic or mixed episodes associated with bipolar disorder, with or without psychotic features (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 extended-release tablets are a valproate and are indicated for the treatment of acute manic or mixed episodes associated with bipolar disorder, with or without psychotic features. A manic episode is a distinct period of abnormally and persistently eleva…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 202419

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

FDA NDC Directory listings under ANDA 202419
Product	Strength	Form · route	Labeler	Product NDC
Divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	Aurobindo Pharma Limited	65862-594
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Aurobindo Pharma Limited	65862-595
Divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	REMEDYREPACK INC.	70518-1781
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	REMEDYREPACK INC.	70518-2003
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-4698
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	72162-2516
Divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	72162-2515
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-4737
Divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-157
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-6074
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-205
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-249
Divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-289
Divalproex sodium	Divalproex sodium 250 mg/1	Tablet, Film coated, Extended releaseOral	NorthStar Rx LLC	16714-484
Divalproex sodium	Divalproex sodium 500 mg/1	Tablet, Film coated, Extended releaseOral	NorthStar Rx LLC	16714-485