NDC codes

FDA NDC Directory
Product NDC (as listed)51407-915Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51407-0915Add 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
51407-915-305140709153030 TABLET, FILM COATED in 1 BOTTLE (51407-915-30)Marketed from May 27, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Vilazodone Hydrochloride
Generic name (nonproprietary)
vilazodone hydrochloride
Active ingredients
Vilazodone hydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208212
Marketing start
Listing expires
Identifiers
Product ID 51407-915_3b8c8c08-ce7c-b237-e063-6294a90aeb14SPL ID 3b8c8c08-ce7c-b237-e063-6294a90aeb14SPL set ID 3b8ca479-72e9-2431-e063-6394a90af7ffRxCUI 1086772, 1086778, 1086784UNII U8HTX2GK8J

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

N451407091530 followed by a unit qualifier and the quantity

Package 51407-0915-30. 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)

Vilazodone hydrochloride tablets are indicated for the treatment of major depressive disorder (MDD) in adults [see Clinical Studies ( 14 )] . Vilazodone hydrochloride tablets are indicated for the treatment of major depressive disorder (MDD) in adults. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208212

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

FDA NDC Directory listings under ANDA 208212
ProductStrengthForm · routeLabelerProduct NDC
Vilazodone HydrochlorideVilazodone hydrochloride 20 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-916
Vilazodone HydrochlorideVilazodone hydrochloride 40 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-917
Vilazodone HydrochlorideVilazodone hydrochloride 40 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-2043
Vilazodone HydrochlorideVilazodone hydrochloride 20 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-2044
Vilazodone HydrochlorideVilazodone hydrochloride 10 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-2045

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Vilazodone Hydrochloride NDC 51407-915 | Med-Code