NDC codes

FDA NDC Directory
Product NDC (as listed)0615-8626Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-8626Add 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
0615-8626-390061586263930 TABLET in 1 BLISTER PACK (0615-8626-39)Marketed from Apr 2, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Haloperidol
Generic name (nonproprietary)
haloperidol
Active ingredients
Haloperidol — 5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216918
Marketing start
Listing expires
Identifiers
Product ID 0615-8626_21b9d026-f029-427f-aa44-1e3f82f5a185SPL ID 21b9d026-f029-427f-aa44-1e3f82f5a185SPL set ID 8743da03-67f1-4cb0-8159-45141cb5466eRxCUI 310672, 314035UNII J6292F8L3D
Pharmacologic class
Typical 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

N400615862639 followed by a unit qualifier and the quantity

Package 00615-8626-39. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 216918

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

FDA NDC Directory listings under ANDA 216918
ProductStrengthForm · routeLabelerProduct NDC
HaloperidolHaloperidol 1 mg/1TabletOralLifestar Pharma LLC70756-002
HaloperidolHaloperidol .5 mg/1TabletOralLifestar Pharma LLC70756-001
HaloperidolHaloperidol 2 mg/1TabletOralLifestar Pharma LLC70756-003
HaloperidolHaloperidol 5 mg/1TabletOralLifestar Pharma LLC70756-004
HaloperidolHaloperidol 10 mg/1TabletOralREMEDYREPACK INC.70518-4725
HaloperidolHaloperidol 10 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8627
HaloperidolHaloperidol 5 mg/1TabletOralREMEDYREPACK INC.70518-4285
HaloperidolHaloperidol 20 mg/1TabletOralLifestar Pharma LLC70756-236
HaloperidolHaloperidol 10 mg/1TabletOralLifestar Pharma LLC70756-242
HaloperidolHaloperidol 2 mg/1TabletOralMajor Pharmaceuticals0904-7504

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