NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4608Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4608Add 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
70518-4608-07051846080050 POUCH in 1 BOX (70518-4608-0) / 1 TABLET in 1 POUCH (70518-4608-1)Marketed from Apr 22, 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)
Rexulti
Generic name (nonproprietary)
brexpiprazole
Active ingredients
Brexpiprazole — 1 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 205422
Marketing start
Listing expires
Identifiers
Product ID 70518-4608_5bc200e6-33a2-16ff-e063-6394a90a12d6SPL ID 5bc200e6-33a2-16ff-e063-6394a90a12d6
Pharmacologic class
Atypical Antipsychotic

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

N470518460800 followed by a unit qualifier and the quantity

Package 70518-4608-00. 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.

Other NDCs under NDA 205422

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

FDA NDC Directory listings under NDA 205422
ProductStrengthForm · routeLabelerProduct NDC
RexultibrexpiprazoleBrexpiprazole 1 mg/1TabletOralOtsuka America Pharmaceutical, Inc.59148-037
RexultibrexpiprazoleBrexpiprazole .25 mg/1TabletOralOtsuka America Pharmaceutical, Inc.59148-035
RexultibrexpiprazoleBrexpiprazole .5 mg/1TabletOralOtsuka America Pharmaceutical, Inc.59148-036
Rexultibrexpiprazole—KitOtsuka America Pharmaceutical, Inc.59148-042
RexultibrexpiprazoleBrexpiprazole 2 mg/1TabletOralOtsuka America Pharmaceutical, Inc.59148-038
RexultibrexpiprazoleBrexpiprazole 3 mg/1TabletOralOtsuka America Pharmaceutical, Inc.59148-039
RexultibrexpiprazoleBrexpiprazole 4 mg/1TabletOralOtsuka America Pharmaceutical, Inc.59148-040
Rexultibrexpiprazole—KitOtsuka America Pharmaceutical, Inc.59148-044
RexultibrexpiprazoleBrexpiprazole 2 mg/1TabletOralREMEDYREPACK INC.70518-3548

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Rexulti (brexpiprazole) NDC 70518-4608 | Med-Code