NDC codes

FDA NDC Directory
Product NDC (as listed)60687-814Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0814Add 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
60687-814-656068708146550 BLISTER PACK in 1 CARTON (60687-814-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-814-11)Marketed from Oct 14, 2024

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)
Prochlorperazine Maleate
Generic name (nonproprietary)
prochlorperazine maleate
Active ingredients
Prochlorperazine maleate — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216598
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 60687-814_5c19032f-9381-7581-e063-6394a90a449aSPL ID 5c19032f-9381-7581-e063-6394a90a449a
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

N460687081465 followed by a unit qualifier and the quantity

Package 60687-0814-65. 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 216598

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

FDA NDC Directory listings under ANDA 216598
ProductStrengthForm · routeLabelerProduct NDC
Prochlorperazine MaleateProchlorperazine maleate 10 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-825
prochlorperazine maleateProchlorperazine maleate 5 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals NY LLC60219-2038
prochlorperazine maleateProchlorperazine maleate 10 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals NY LLC60219-2039

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