NDC codes

FDA NDC Directory
Product NDC (as listed)27808-222Labeler and product segments. Claims need a package NDC.
Product NDC at billing width27808-0222Add 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
27808-222-012780802220130 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-222-01)Marketed from Oct 25, 2021

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)
Paliperidone
Generic name (nonproprietary)
paliperidone
Active ingredients
Paliperidone — 1.5 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212807
Marketing start
Listing expires
Identifiers
Product ID 27808-222_ffd2bfbd-11f5-436a-9ebf-bbd4ef92bacdSPL ID ffd2bfbd-11f5-436a-9ebf-bbd4ef92bacdSPL set ID d7033e52-3df2-48e2-adda-15a57c2f148fRxCUI 672567, 672569, 672571, 866103UNII 838F01T721
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

N427808022201 followed by a unit qualifier and the quantity

Package 27808-0222-01. 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)

Paliperidone is an atypical antipsychotic agent indicated for Treatment of schizophrenia ( 1.1 ) Adults: Efficacy was established in three 6-week trials and one maintenance trial. ( 14.1 ) Adolescents (ages 12 to 17): Efficacy was established in one 6-week trial. ( 14.1 ) Treatment of schizoaffective disorder as monotherapy and as an adjunct to mood stabilizers and/or antidepressants. ( 1.2 ) Efficacy was established in two 6-week trials in adult patients. ( 14.2 ) 1.1 Schizophrenia Paliperidone extended-release tablets are indicated for the treatment of schizophrenia [see Clinical Studies (14.1) ] . The efficacy of paliperidone extended-release tablets in schizophrenia was established in th…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 212807

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

FDA NDC Directory listings under ANDA 212807
ProductStrengthForm · routeLabelerProduct NDC
PaliperidonePaliperidone 9 mg/1Tablet, Extended releaseOralTris Pharma Inc27808-225
PaliperidonePaliperidone 3 mg/1Tablet, Extended releaseOralTris Pharma Inc27808-223
PaliperidonePaliperidone 6 mg/1Tablet, Extended releaseOralTris Pharma Inc27808-224

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