NDC codes

FDA NDC Directory
Product NDC (as listed)51079-736Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51079-0736Add 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
51079-736-205107907362051079073620100 BLISTER PACK in 1 CARTON (51079-736-20) / 1 TABLET in 1 BLISTER PACK (51079-736-01)Marketed from Feb 15, 2004

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
Mylan Institutional Inc.NDC labeler code 51079
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070278
Marketing start
Listing expires
Identifiers
Product ID 51079-736_3dd4fea4-d455-5a4d-e063-6394a90ab14cSPL ID 3dd4fea4-d455-5a4d-e063-6394a90ab14cSPL set ID ad7d2f17-a4e8-4ebc-9baf-5983ac626782RxCUI 310670, 310671, 310672, 314034, 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

N451079073620 followed by a unit qualifier and the quantity

Package 51079-0736-20. 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.

Full label on DailyMed (opens in a new tab)

About NDC 51079-736

What is NDC 51079-736?
51079-736 is the product NDC for Haloperidol, Haloperidol 5 mg/1 tablet, listed with the FDA by Mylan Institutional 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?
Mylan Institutional Inc., NDC labeler code 51079. 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.

Other finished products listed under the same name: strengths, forms and labelers.

Other Haloperidol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
HaloperidolHaloperidol .5 mg/1TabletOralAjanta Pharma USA Inc.27241-26427241-0264-01
HaloperidolHaloperidol 1 mg/1TabletOralAjanta Pharma USA Inc.27241-26527241-0265-01
HaloperidolHaloperidol 2 mg/1TabletOralAjanta Pharma USA Inc.27241-26627241-0266-01
HaloperidolHaloperidol 5 mg/1TabletOralAjanta Pharma USA Inc.27241-26727241-0267-01
HaloperidolHaloperidol 10 mg/1TabletOralAjanta Pharma USA Inc.27241-26827241-0268-01
HaloperidolHaloperidol 20 mg/1TabletOralAjanta Pharma USA Inc.27241-26927241-0269-01
HaloperidolHaloperidol 10 mg/1TabletOralREMEDYREPACK INC.70518-472570518-4725-00
HaloperidolHaloperidol 5 mg/1TabletOralCoupler LLC67046-032967046-0329-03
HaloperidolHaloperidol 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-03787441-0037-01
HaloperidolHaloperidol .5 mg/1TabletOralSafecor Health, LLC48433-15148433-0151-20

All 171 Haloperidol NDCs

Other NDCs under ANDA 070278

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

FDA NDC Directory listings under ANDA 070278
ProductStrengthForm · routeLabelerProduct NDC
HaloperidolHaloperidol 2 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0214
HaloperidolHaloperidol 1 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0257
HaloperidolHaloperidol 5 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0327
HaloperidolHaloperidol .5 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0351
HaloperidolHaloperidol .5 mg/1TabletOralMylan Institutional Inc.51079-733
HaloperidolHaloperidol 1 mg/1TabletOralMylan Institutional Inc.51079-734
HaloperidolHaloperidol 2 mg/1TabletOralMylan Institutional Inc.51079-735
HaloperidolHaloperidol 5 mg/1TabletOralCardinal Health 107, LLC55154-5059
HaloperidolHaloperidol .5 mg/1TabletOralCoupler LLC67046-1496

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