What is NDC 70518-4267?

70518-4267 is the product NDC for Paliperidone, Paliperidone 9 mg/1 tablet, extended release, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Paliperidone?

64 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Paliperidone NDC 70518-4267 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4267Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4267Add 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
70518-4267-0	7051842670070518426700	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4267-0)Marketed from Jan 27, 2025
70518-4267-1	7051842670170518426701	30 POUCH in 1 BOX (70518-4267-1) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-4267-2)Marketed from Jan 28, 2025

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): Paliperidone
Generic name (nonproprietary): paliperidone
Active ingredients: Paliperidone — 9 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205618
Marketing start: Jan 27, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 70518-4267_400ab61f-5daf-6925-e063-6394a90ae1f6SPL ID 400ab61f-5daf-6925-e063-6394a90ae1f6SPL set ID f13d3678-a861-42ba-be44-0d89f1b66ef3RxCUI 672571UNII 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

N470518426700 followed by a unit qualifier and the quantity

Package 70518-4267-00. 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

Current FDA label (SPL), effective Sep 30, 2025. 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 ofpaliperidone extended-release tabletsin schizophrenia was established i…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4267

What is NDC 70518-4267?: 70518-4267 is the product NDC for Paliperidone, Paliperidone 9 mg/1 tablet, extended release, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Paliperidone.
What is the active ingredient?: Paliperidone.
Who is the labeler?: REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Paliperidone?: 64 other product NDCs are listed under this name. See all Paliperidone 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 Paliperidone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Paliperidone	Paliperidone 6 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1630	67046-1630-03
Paliperidone	Paliperidone 1.5 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-432	69367-0432-30
Paliperidone	Paliperidone 3 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-433	69367-0433-30
Paliperidone	Paliperidone 6 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-434	69367-0434-30
Paliperidone	Paliperidone 9 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-435	69367-0435-30
Paliperidone	Paliperidone 1.5 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2648	72162-2648-03
Paliperidone	Paliperidone 3 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2649	72162-2649-03
Paliperidone	Paliperidone 6 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2650	72162-2650-03
Paliperidone	Paliperidone 9 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2651	72162-2651-03
Paliperidone	Paliperidone 1.5 mg/1	Tablet, Extended releaseOral	Eskayef Pharmaceuticals Limited	72658-1253	72658-1253-0172658-1253-0272658-1253-03

All 65 Paliperidone NDCs

Other NDCs under ANDA 205618

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

FDA NDC Directory listings under ANDA 205618
Product	Strength	Form · route	Labeler	Product NDC
Paliperidone	Paliperidone 1.5 mg/1	Tablet, Film coated, Extended releaseOral	NorthStar RxLLC	16714-866
Paliperidone	Paliperidone 9 mg/1	Tablet, Film coated, Extended releaseOral	NorthStar RxLLC	16714-869
Paliperidone	Paliperidone 3 mg/1	Tablet, Film coated, Extended releaseOral	NorthStar RxLLC	16714-867
Paliperidone	Paliperidone 6 mg/1	Tablet, Film coated, Extended releaseOral	NorthStar RxLLC	16714-868
Paliperidone	Paliperidone 3 mg/1	Tablet, Extended releaseOral	American Health Packaging	60687-459
Paliperidone	Paliperidone 6 mg/1	Tablet, Extended releaseOral	American Health Packaging	60687-470
Paliperidone	Paliperidone 3 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6935
Paliperidone	Paliperidone 6 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6936
Paliperidone	Paliperidone 9 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6937
Paliperidone	Paliperidone 1.5 mg/1	Tablet, Film coated, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-744
Paliperidone	Paliperidone 6 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4268
Paliperidone	Paliperidone 3 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4269
Paliperidone	Paliperidone 6 mg/1	Tablet, Film coated, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-766
Paliperidone	Paliperidone 3 mg/1	Tablet, Film coated, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-765
Paliperidone	Paliperidone 9 mg/1	Tablet, Film coated, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-767