What is NDC 67296-2342?

67296-2342 is the product NDC for Prochlorperazine Maleate, Prochlorperazine maleate 10 mg/1 tablet, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.

Redpharm Drug, NDC labeler code 67296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Prochlorperazine Maleate?

61 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Prochlorperazine Maleate NDC 67296-2342

NDC codes

FDA NDC Directory

Product NDC (as listed)67296-2342Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67296-2342Add 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
67296-2342-4	6729623420467296234204	15 TABLET in 1 BOTTLE (67296-2342-4)Marketed from Sep 7, 2023

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): Prochlorperazine Maleate
Generic name (nonproprietary): prochlorperazine maleate
Active ingredients: Prochlorperazine maleate — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Redpharm DrugNDC labeler code 67296
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216202
Marketing start: Sep 7, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Phenothiazines (Chemical structure)
Identifiers: Product ID 67296-2342_5d769974-1435-907d-e063-6394a90ac3afSPL ID 5d769974-1435-907d-e063-6394a90ac3af
Pharmacologic class: Phenothiazine

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

N467296234204 followed by a unit qualifier and the quantity

Package 67296-2342-04. 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.

About NDC 67296-2342

What is NDC 67296-2342?: 67296-2342 is the product NDC for Prochlorperazine Maleate, Prochlorperazine maleate 10 mg/1 tablet, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Prochlorperazine Maleate.
What is the active ingredient?: Prochlorperazine maleate.
Who is the labeler?: Redpharm Drug, NDC labeler code 67296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Prochlorperazine Maleate?: 61 other product NDCs are listed under this name. See all Prochlorperazine Maleate 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 Prochlorperazine Maleate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
prochlorperazine maleate	Prochlorperazine maleate 5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4728	70518-4728-00
Prochlorperazine Maleate	Prochlorperazine maleate 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4498	70518-4498-00
prochlorperazine maleate	Prochlorperazine maleate 5 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-773	59651-0773-01
prochlorperazine maleate	Prochlorperazine maleate 10 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-774	59651-0774-01
Prochlorperazine Maleate	Prochlorperazine maleate 5 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-517	72789-0517-0172789-0517-90
Prochlorperazine Maleate	Prochlorperazine maleate 10 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-518	72789-0518-0172789-0518-1572789-0518-90
Prochlorperazine Maleate	Prochlorperazine maleate 5 mg/1	Tablet, Film coatedOral	Leading Pharma, LLC	69315-265	69315-0265-01
Prochlorperazine Maleate	Prochlorperazine maleate 10 mg/1	Tablet, Film coatedOral	Leading Pharma, LLC	69315-266	69315-0266-01
Prochlorperazine Maleate	Prochlorperazine maleate 10 mg/1	TabletOral	GLENMARK PHARMACEUTICALS INC., USA	68462-947	68462-0947-0168462-0947-10
Prochlorperazine Maleate	Prochlorperazine maleate 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4319	70518-4319-00

All 62 Prochlorperazine Maleate NDCs

Other NDCs under ANDA 216202

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

FDA NDC Directory listings under ANDA 216202
Product	Strength	Form · route	Labeler	Product NDC
Prochlorperazine Maleate	Prochlorperazine maleate 5 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7381
Prochlorperazine Maleate	Prochlorperazine maleate 10 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7382
Prochlorperazine Maleate	Prochlorperazine maleate 5 mg/1	Tablet, Film coatedOral	ANI Pharmaceuticals, Inc.	70954-688
Prochlorperazine Maleate	Prochlorperazine maleate 10 mg/1	Tablet, Film coatedOral	ANI Pharmaceuticals, Inc.	70954-689
Prochlorperazine Maleate	Prochlorperazine maleate 10 mg/1	TabletOral	Northstar Rx LLC	72603-169