Prescription drug · ANDA
Haloperidol NDC 72789-566
Haloperidol .5 mg/1 · Tablet · Oral · PD-Rx Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72789-566-01 | 7278905660172789056601 | 100 TABLET in 1 BOTTLE, PLASTIC (72789-566-01)Marketed from Apr 22, 2026 |
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)
- Haloperidol
- Generic name (nonproprietary)
- haloperidol
- Active ingredients
- Haloperidol — .5 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 071130
- Marketing start
- Listing expires
- Identifiers
- Product ID 72789-566_50221596-087a-9973-e063-6394a90ae95fSPL ID 50221596-087a-9973-e063-6394a90ae95fSPL set ID 533b0b4c-cbd6-4ec0-a333-8b04b5b43a1dRxCUI 197754, 310670, 310671, 310672, 314034, 314035UNII J6292F8L3DUPC 0372789566016, 0372789559018, 0372789569017, 0372789568010, 0372789558011, 0372789567013
- 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
N472789056601followed by a unit qualifier and the quantityPackage 72789-0566-01. 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)
INDICATIONS AND USAGE Haloperidol tablets are indicated for use in the management of manifestations of psychotic disorders. Haloperidol tablets are indicated for the control of tics and vocal utterances of Tourette’s Disorder in children and adults. Haloperidol tablets are effective for the treatment of severe behavior problems in children of combative, explosive hyperexcitability (which cannot be accounted for by immediate provocation). Haloperidol tablets are also effective in the short-term treatment of hyperactive children who show excessive motor activity with accompanying conduct disorders consisting of some or all of the following symptoms: impulsivity, difficulty sustaining attention…
Excerpt only. Read the full label for complete information.
About NDC 72789-566
- What is NDC 72789-566?
- 72789-566 is the product NDC for Haloperidol, Haloperidol .5 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Haloperidol.
- What is the active ingredient?
- Haloperidol.
- Who is the labeler?
- PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Haloperidol?
- 170 other product NDCs are listed under this name. See all Haloperidol NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Haloperidol products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Haloperidol | Haloperidol .5 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-264 | 27241-0264-01 |
| Haloperidol | Haloperidol 1 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-265 | 27241-0265-01 |
| Haloperidol | Haloperidol 2 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-266 | 27241-0266-01 |
| Haloperidol | Haloperidol 5 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-267 | 27241-0267-01 |
| Haloperidol | Haloperidol 10 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-268 | 27241-0268-01 |
| Haloperidol | Haloperidol 20 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-269 | 27241-0269-01 |
| Haloperidol | Haloperidol 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4725 | 70518-4725-00 |
| Haloperidol | Haloperidol 5 mg/1 | TabletOral | Coupler LLC | 67046-0329 | 67046-0329-03 |
| Haloperidol | Haloperidol 5 mg/1 | TabletOral | Unit Dose Solutions, Inc. | 87441-037 | 87441-0037-01 |
| Haloperidol | Haloperidol .5 mg/1 | TabletOral | Safecor Health, LLC | 48433-151 | 48433-0151-20 |
Other NDCs under ANDA 071130
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Haloperidol | Haloperidol .5 mg/1 | TabletOral | AiPing Pharmaceutical, Inc | 11788-071 |
| Haloperidol | Haloperidol 1 mg/1 | TabletOral | AiPing Pharmaceutical, Inc | 11788-072 |
| Haloperidol | Haloperidol 2 mg/1 | TabletOral | AiPing Pharmaceutical, Inc | 11788-073 |
| Haloperidol | Haloperidol 5 mg/1 | TabletOral | AiPing Pharmaceutical, Inc | 11788-074 |
| Haloperidol | Haloperidol 10 mg/1 | TabletOral | AiPing Pharmaceutical, Inc | 11788-075 |
| Haloperidol | Haloperidol 20 mg/1 | TabletOral | AiPing Pharmaceutical, Inc | 11788-076 |
| Haloperidol | Haloperidol 5 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-558 |
| Haloperidol | Haloperidol 10 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-559 |
| Haloperidol | Haloperidol 1 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-567 |
| Haloperidol | Haloperidol 2 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-568 |
| Haloperidol | Haloperidol 20 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-569 |