NDC codes

FDA NDC Directory
Product NDC (as listed)0904-7621Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00904-7621Add 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
0904-7621-720090476217210 TRAY in 1 CASE (0904-7621-72) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0904-7621-66)Marketed from Aug 3, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 acid — 500 mg/10mL
Dosage form
Solution
Route
Oral
Labeler
Major PharmaceuticalsNDC labeler code 0904
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075379
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 0904-7621_3aea592e-0fb0-4853-83d1-41b2d13c5302SPL ID 3aea592e-0fb0-4853-83d1-41b2d13c5302SPL set ID a33f7657-ad0f-43e9-ba48-024746e6d08eRxCUI 1099687UNII 614OI1Z5WIUPC 0309047621668, 0309047620418
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

N400904762172 followed by a unit qualifier and the quantity

Package 00904-7621-72. 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 is 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 is 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 is 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 absence seizures. Simple absenc…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0904-7621

What is NDC 0904-7621?
0904-7621 is the product NDC for Valproic Acid, Valproic acid 500 mg/10mL solution, listed with the FDA by Major Pharmaceuticals. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Valproic Acid.
What is the active ingredient?
Valproic acid.
Who is the labeler?
Major Pharmaceuticals, NDC labeler code 0904. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Valproic Acid?
27 other product NDCs are listed under this name. See all Valproic Acid 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 Valproic Acid NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Valproic AcidValproic acid 250 mg/5mLSolutionOralAmerican Health Packaging60687-94260687-0942-1760687-0942-77
Valproic AcidValproic acid 500 mg/10mLSolutionOralAmerican Health Packaging60687-95360687-0953-56
Valproic AcidValproic acid 250 mg/5mLSolutionOralMajor Pharmaceuticals0904-762000904-7620-7000904-7620-94
Valproic AcidValproic acid 250 mg/5mLSolutionOralREMEDYREPACK INC.70518-429870518-4298-0070518-4298-0270518-4298-04
Valproic AcidValproic acid 250 mg/5mLSolutionOralNorthStar Rx LLC72603-25372603-0253-01
Valproic AcidValproic acid 250 mg/5mLSolutionOralQUAGEN PHARMACEUTICALS LLC70752-20270752-0202-12
Valproic AcidValproic acid 250 mg/5mLSolutionOralANI Pharmaceuticals, Inc.62559-26662559-0266-16
Valproic AcidValproic acid 250 mg/5mLSolutionOralKesin Pharma Corporation81033-26681033-0266-5081033-0266-52
Valproic AcidValproic acid 250 mg/5mLSolutionOralREMEDYREPACK INC.70518-380570518-3805-0070518-3805-02
Valproic AcidValproic acid 250 mg/1CapsuleOralDirect_Rx72189-01072189-0010-30

All 28 Valproic Acid NDCs

Other NDCs under ANDA 075379

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

FDA NDC Directory listings under ANDA 075379
ProductStrengthForm · routeLabelerProduct NDC
Valproic AcidValproic acid 250 mg/5mLSolutionOralMajor Pharmaceuticals0904-7620
Valproic AcidValproic acid 250 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-0675
Valproic AcidValproic acid 250 mg/5mLSolutionOralREMEDYREPACK INC.70518-3805
Valproic AcidValproic acid 250 mg/5mLSolutionOralAmerican Health Packaging60687-942
Valproic AcidValproic acid 500 mg/10mLSolutionOralAmerican Health Packaging60687-953
Valproic AcidValproic acid 250 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-4675
Valproic AcidValproic acid 500 mg/10mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-1350
Valproic AcidValproic acid 250 mg/5mLSolutionOralBryant Ranch Prepack71335-2250

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