NDC codes

FDA NDC Directory
Product NDC (as listed)70518-0079Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-0079Add 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
70518-0079-0705180079007051800790030 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (70518-0079-0)Marketed from Dec 23, 2016
70518-0079-17051800790170518007901100 POUCH in 1 BOX (70518-0079-1) / 1 CAPSULE, LIQUID FILLED in 1 POUCH (70518-0079-2)Marketed from Jun 11, 2020
70518-0079-3705180079037051800790350 POUCH in 1 BOX (70518-0079-3) / 1 CAPSULE, LIQUID FILLED in 1 POUCH (70518-0079-2)Marketed from Apr 23, 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)
Valproic Acid
Generic name (nonproprietary)
valproic acid
Active ingredients
Valproic acid — 250 mg/1
Dosage form
Capsule, Liquid filled
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
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 70518-0079_5c021a3b-84b2-1581-e063-6394a90a5a58SPL ID 5c021a3b-84b2-1581-e063-6394a90a5a58
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

N470518007900 followed by a unit qualifier and the quantity

Package 70518-0079-00. 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.

About NDC 70518-0079

What is NDC 70518-0079?
70518-0079 is the product NDC for Valproic Acid, Valproic acid 250 mg/1 capsule, liquid filled, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, 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?
REMEDYREPACK INC., NDC labeler code 70518. 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 500 mg/10mLSolutionOralMajor Pharmaceuticals0904-762100904-7621-72
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

All 28 Valproic Acid NDCs

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 filledOralATLANTIC BIOLOGICALS CORP.17856-0152
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralAphena Pharma Solutions - Tennessee, LLC43353-279
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralBryant Ranch Prepack63629-2454
Valproic AcidValproic acid 250 mg/1Capsule, Liquid filledOralBionpharma Inc.69452-150

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