Prescription drug · ANDA

divalproex sodium NDC 70518-4553

Divalproex sodium 500 mg/1 · Tablet, Film coated, Extended release · Oral · REMEDYREPACK INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4553Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4553Add 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 NDC11-digit (billing)PackageCopy
70518-4553-07051845530030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4553-0)Marketed from Jan 21, 2026

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214643
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 70518-4553_5b9da891-ab9d-45ea-e063-6394a90a1539SPL ID 5b9da891-ab9d-45ea-e063-6394a90a1539
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

N470518455300 followed by a unit qualifier and the quantity

Package 70518-4553-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 214643

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

FDA NDC Directory listings under ANDA 214643
ProductStrengthForm · routeLabelerProduct NDC
divalproex sodiumDivalproex sodium 500 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-7841
divalproex sodiumDivalproex sodium 250 mg/1Tablet, Film coated, Extended releaseOralAmerican Health Packaging60687-904
divalproex sodiumDivalproex sodium 500 mg/1Tablet, Film coated, Extended releaseOralAmerican Health Packaging60687-915
divalproex sodiumDivalproex sodium 250 mg/1Tablet, Film coated, Extended releaseOralREMEDYREPACK INC.70518-4557
divalproex sodiumDivalproex sodium 500 mg/1Tablet, Film coated, Extended releaseOralCoupler LLC67046-1595
divalproex sodiumDivalproex sodium 250 mg/1Tablet, Film coated, Extended releaseOralBluePoint Laboratories68001-646
divalproex sodiumDivalproex sodium 250 mg/1Tablet, Film coated, Extended releaseOralUnichem Pharmaceuticals (USA), Inc.29300-380
divalproex sodiumDivalproex sodium 500 mg/1Tablet, Film coated, Extended releaseOralBluePoint Laboratories68001-647
divalproex sodiumDivalproex sodium 500 mg/1Tablet, Film coated, Extended releaseOralUnichem Pharmaceuticals (USA), Inc.29300-381
divalproex sodiumDivalproex sodium 500 mg/1Tablet, Film coated, Extended releaseOralCoupler LLC67046-1631

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divalproex sodium NDC 70518-4553 | Med-Code