NDC codes

FDA NDC Directory
Product NDC (as listed)72205-262Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72205-0262Add 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
72205-262-307220502623030 TABLET in 1 BOTTLE (72205-262-30)Marketed from Jul 14, 2023

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 hydrochloride40 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208228
Marketing start
Listing expires
Identifiers
Product ID 72205-262_c3e167cd-7f56-45eb-80df-a60fa1392e57SPL ID c3e167cd-7f56-45eb-80df-a60fa1392e57SPL set ID c3e167cd-7f56-45eb-80df-a60fa1392e57RxCUI 1086772, 1086778, 1086784UNII U8HTX2GK8JUPC 0372205262300, 0372205261303, 0372205260306

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

N472205026230 followed by a unit qualifier and the quantity

Package 72205-0262-30. 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 208228

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

FDA NDC Directory listings under ANDA 208228
ProductStrengthForm · routeLabelerProduct NDC
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralProficient Rx LP82804-128
vilazodone hydrochlorideVilazodone hydrochloride 20 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-261
vilazodone hydrochlorideVilazodone hydrochloride 10 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-260
vilazodone hydrochlorideVilazodone hydrochloride 20 mg/1TabletOralApotex Corp.60505-4373
vilazodone hydrochlorideVilazodone hydrochloride 10 mg/1TabletOralApotex Corp.60505-4372
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralApotex Corp.60505-4374
vilazodone hydrochlorideVilazodone hydrochloride 10 mg/1TabletOralNorthstar Rx LLC72603-813
vilazodone hydrochlorideVilazodone hydrochloride 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8734
vilazodone hydrochlorideVilazodone hydrochloride 20 mg/1TabletOralNorthstar Rx LLC72603-814
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8735
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralNorthstar Rx LLC72603-815

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