Prochlorperazine NDC 0713-0135

NDC codes

FDA NDC Directory

Product NDC (as listed)0713-0135Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00713-0135Add 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
0713-0135-10	00713013510	1000 BLISTER PACK in 1 CARTON (0713-0135-10) / 1 SUPPOSITORY in 1 BLISTER PACKMarketed from Nov 30, 1993
0713-0135-12	00713013512	12 BLISTER PACK in 1 CARTON (0713-0135-12) / 1 SUPPOSITORY in 1 BLISTER PACKMarketed from Nov 30, 1993

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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
Generic name (nonproprietary): prochlorperazine
Active ingredients: Prochlorperazine — 25 mg/1
Dosage form: Suppository
Route: Rectal
Labeler: Cosette Pharmaceuticals, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040058
Marketing start: Nov 30, 1993
Listing expires: Dec 31, 2026
Other FDA classes: Phenothiazines (Chemical structure)
Identifiers: Product ID 0713-0135_462a6c34-db6d-8d31-e063-6294a90ae196SPL ID 462a6c34-db6d-8d31-e063-6294a90ae196SPL set ID 9595346e-76e5-e155-341b-ffaaafb885abRxCUI 198159UNII YHP6YLT61T
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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N400713013510 followed by a unit qualifier and the quantity

Package 00713-0135-10. 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 Dec 17, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Prochlorperazine Suppositories, USP 25 mg are indicated in the control of severe nausea and vomiting in adults.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)