Prescription drug · ANDA

vilazodone hydrochloride NDC 60505-4372

Vilazodone hydrochloride 10 mg/1 · Tablet · Oral · Apotex Corp.

NDC codes

FDA NDC Directory
Product NDC (as listed)60505-4372Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60505-4372Add 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
60505-4372-36050543720330 TABLET in 1 BOTTLE (60505-4372-3)Marketed from Oct 26, 2023

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)
vilazodone hydrochloride
Generic name (nonproprietary)
vilazodone hydrochloride
Active ingredients
Vilazodone hydrochloride — 10 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 60505-4372_f7ed5f37-5a34-4888-b659-8fe1139f646dSPL ID f7ed5f37-5a34-4888-b659-8fe1139f646d

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

N460505437203 followed by a unit qualifier and the quantity

Package 60505-4372-03. 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.

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 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8734
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8735
vilazodone hydrochlorideVilazodone hydrochloride 10 mg/1TabletOralNorthstar Rx LLC72603-813
vilazodone hydrochlorideVilazodone hydrochloride 20 mg/1TabletOralNorthstar Rx LLC72603-814
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralNorthstar Rx LLC72603-815
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-262
vilazodone hydrochlorideVilazodone hydrochloride 10 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-260
vilazodone hydrochlorideVilazodone hydrochloride 20 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-261
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralProficient Rx LP82804-128
vilazodone hydrochlorideVilazodone hydrochloride 20 mg/1TabletOralApotex Corp.60505-4373
vilazodone hydrochlorideVilazodone hydrochloride 40 mg/1TabletOralApotex Corp.60505-4374

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