NDC codes

FDA NDC Directory
Product NDC (as listed)17856-0152Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17856-0152Add 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
17856-0152-117856015201100 POUCH in 1 BOX, UNIT-DOSE (17856-0152-1) / 1 CAPSULE, LIQUID FILLED in 1 POUCHMarketed from Jun 25, 2021

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)
Valproic Acid
Generic name (nonproprietary)
valproic acid
Active ingredients
Valproic acid250 mg/1
Dosage form
Capsule, Liquid filled
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 073484
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 17856-0152_38930d1f-1f70-1fa5-e063-6394a90a5c21SPL ID 38930d1f-1f70-1fa5-e063-6394a90a5c21SPL set ID 453444b6-1f50-49de-ab3c-1e429c83bffaRxCUI 1099681UNII 614OI1Z5WI
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

N417856015201 followed by a unit qualifier and the quantity

Package 17856-0152-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Valproic Acid Capsules are indicated for: Monotherapy and adjunctive therapy of complex partial seizures; sole and adjunctive therapy of simple and complex absence seizures; adjunctive therapy in patients with multiple seizure types that include absence seizures ( 1 ) 1.1 Epilepsy Valproic Acid Capsules are indicated as monotherapy and adjunctive therapy in the treatment of patients with complex partial seizures that occur either in isolation or in association with other types of seizures. Valproic Acid Capsules are indicated for use as sole and adjunctive therapy in the treatment of simple and complex absence seizures, and adjunctively in patients with multiple seizure types which include a

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 073484

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

FDA NDC Directory listings under ANDA 073484
ProductStrengthForm · routeLabelerProduct NDC
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8205
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralAphena Pharma Solutions - Tennessee, LLC43353-279
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralBionpharma Inc.69452-150
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralBryant Ranch Prepack63629-2454
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralREMEDYREPACK INC.70518-0079

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