Tetrabenazine NDC 60505-3882

NDC codes

FDA NDC Directory

Product NDC (as listed)60505-3882Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60505-3882Add 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 NDC	11-digit (billing)	Package	Copy
60505-3882-7	60505388207	112 TABLET in 1 BOTTLE (60505-3882-7)Marketed from Jun 18, 2020

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): Tetrabenazine
Generic name (nonproprietary): tetrabenazine
Active ingredients: Tetrabenazine — 12.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Apotex Corp.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206093
Marketing start: Jun 18, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Vesicular Monoamine Transporter 2 Inhibitors (Mechanism)
Identifiers: Product ID 60505-3882_28a5d355-8681-d49f-0db3-c1da5316e1a2SPL ID 28a5d355-8681-d49f-0db3-c1da5316e1a2
Pharmacologic class: Vesicular Monoamine Transporter 2 Inhibitor

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

N460505388207 followed by a unit qualifier and the quantity

Package 60505-3882-07. 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 206093

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

FDA NDC Directory listings under ANDA 206093
Product	Strength	Form · route	Labeler	Product NDC
Tetrabenazine	Tetrabenazine 12.5 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-480
Tetrabenazine	Tetrabenazine 25 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-481
Tetrabenazine	Tetrabenazine 25 mg/1	TabletOral	Apotex Corp.	60505-3883