Risperidone NDC 50090-3340

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-3340Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-3340Add 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 NDC	11-digit (billing)	Package	Copy
50090-3340-0	50090334000	30 TABLET in 1 BOTTLE (50090-3340-0)Marketed from Jan 22, 2018

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): Risperidone
Generic name (nonproprietary): risperidone
Active ingredients: Risperidone — 2 mg/1
Dosage form: Tablet
Route: Oral
Labeler: A-S Medication Solutions
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 201003
Marketing start: Mar 28, 2014
Listing expires: Dec 31, 2027
Identifiers: Product ID 50090-3340_0e5fb718-a235-47e3-9ef7-9399f1b07894SPL ID 0e5fb718-a235-47e3-9ef7-9399f1b07894
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

N450090334000 followed by a unit qualifier and the quantity

Package 50090-3340-00. 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 ANDA 201003

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

FDA NDC Directory listings under ANDA 201003
Product	Strength	Form · route	Labeler	Product NDC
Risperidone	Risperidone .5 mg/1	TabletOral	Proficient Rx LP	63187-642
Risperidone	Risperidone 1 mg/1	TabletOral	Proficient Rx LP	63187-264
Risperidone	Risperidone 1 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-908
Risperidone	Risperidone 2 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4618
Risperidone	Risperidone 1 mg/1	TabletOral	A-S Medication Solutions	50090-3341
Risperidone	Risperidone 2 mg/1	TabletOral	Bryant Ranch Prepack	71335-0459
Risperidone	Risperidone .5 mg/1	TabletOral	A-S Medication Solutions	50090-3344
Risperidone	Risperidone 2 mg/1	TabletOral	Coupler LLC	67046-0630
Risperidone	Risperidone 1 mg/1	TabletOral	Coupler LLC	67046-0635
Risperidone	Risperidone .5 mg/1	TabletOral	Coupler LLC	67046-0644
Risperidone	Risperidone 2 mg/1	TabletOral	Proficient Rx LP	63187-439
Risperidone	Risperidone 1 mg/1	TabletOral	Bryant Ranch Prepack	71335-0626
Risperidone	Risperidone 3 mg/1	TabletOral	Direct_Rx	72189-525
Risperidone	Risperidone 4 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-246
Risperidone	Risperidone 3 mg/1	TabletOral	REMEDYREPACK INC.	70518-1502
Risperidone	Risperidone 2 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-264
Risperidone	Risperidone .5 mg/1	TabletOral	REMEDYREPACK INC.	70518-1575
Risperidone	Risperidone .5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0130
Risperidone	Risperidone .25 mg/1	TabletOral	Bryant Ranch Prepack	71335-0740
Risperidone	Risperidone 2 mg/1	TabletOral	REMEDYREPACK INC.	70518-1568

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