Prescription drug · ANDA

Prochlorperazine Maleate NDC 70518-4498

Prochlorperazine maleate 5 mg/1 · Tablet · Oral · REMEDYREPACK INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4498Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4498Add 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
70518-4498-07051844980020 TABLET in 1 BOTTLE, PLASTIC (70518-4498-0)Marketed from Oct 11, 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)
Prochlorperazine Maleate
Generic name (nonproprietary)
prochlorperazine maleate
Active ingredients
Prochlorperazine maleate — 5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217478
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 70518-4498_5b74d0eb-b819-95c0-e063-6294a90a6380SPL ID 5b74d0eb-b819-95c0-e063-6294a90a6380
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

N470518449800 followed by a unit qualifier and the quantity

Package 70518-4498-00. 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 217478

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

FDA NDC Directory listings under ANDA 217478
ProductStrengthForm · routeLabelerProduct NDC
Prochlorperazine MaleateProchlorperazine maleate 5 mg/1Tablet, Film coatedOralRedpharm Drug67296-2099
Prochlorperazine MaleateProchlorperazine maleate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2621
Prochlorperazine MaleateProchlorperazine maleate 5 mg/1TabletOralA-S Medication Solutions50090-7634
Prochlorperazine MaleateProchlorperazine maleate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2386
Prochlorperazine MaleateProchlorperazine maleate 5 mg/1TabletOralBionpharma Inc.69452-471
Prochlorperazine MaleateProchlorperazine maleate 10 mg/1TabletOralBionpharma Inc.69452-472
Prochlorperazine MaleateProchlorperazine maleate 5 mg/1TabletOralRedpharm Drug67296-2178
Prochlorperazine MaleateProchlorperazine maleate 5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7147
Prochlorperazine MaleateProchlorperazine maleate 10 mg/1TabletOralRedpharm Drug67296-2195
Prochlorperazine MaleateProchlorperazine maleate 10 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8708
Prochlorperazine MaleateProchlorperazine maleate 5 mg/1Tablet, Film coatedOralBionpharma Inc.69452-309
Prochlorperazine MaleateProchlorperazine maleate 10 mg/1Tablet, Film coatedOralBionpharma Inc.69452-310

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Prochlorperazine Maleate NDC 70518-4498 | Med-Code