NDC codes

FDA NDC Directory
Product NDC (as listed)68084-272Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68084-0272Add 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
68084-272-0168084027201100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-272-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-272-11)Marketed from Dec 2, 2008

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)
Risperidone
Generic name (nonproprietary)
risperidone
Active ingredients
Risperidone — 1 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078040
Marketing start
Listing expires
Identifiers
Product ID 68084-272_43e5e95c-ad0c-3657-e063-6394a90af632SPL ID 43e5e95c-ad0c-3657-e063-6394a90af632SPL set ID f11dae15-b057-4258-9229-3819d0c980feRxCUI 312828, 312829, 312830, 312831, 312832, 314211UNII L6UH7ZF8HC
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

N468084027201 followed by a unit qualifier and the quantity

Package 68084-0272-01. 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

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

Other NDCs under ANDA 078040

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

FDA NDC Directory listings under ANDA 078040
ProductStrengthForm · routeLabelerProduct NDC
risperidoneRisperidone 3 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-669
risperidoneRisperidone .5 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-666
risperidoneRisperidone 1 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-667
risperidoneRisperidone 2 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-668
risperidoneRisperidone 4 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-670
RisperidoneRisperidone 2 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-273
RisperidoneRisperidone .25 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-270
RisperidoneRisperidone .5 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-271
RisperidoneRisperidone 3 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-274
RisperidoneRisperidone 4 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-277
risperidoneRisperidone .25 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7360
risperidoneRisperidone .5 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-0180
risperidoneRisperidone .5 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7361
risperidoneRisperidone 1 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7362
risperidoneRisperidone .25 mg/1Tablet, Film coatedOralProficient Rx LP63187-418
risperidoneRisperidone 2 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7363
risperidoneRisperidone 3 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7364
risperidoneRisperidone 4 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7365
risperidoneRisperidone 1 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-114
risperidoneRisperidone .25 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-112

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