Prochlorperazine 10 MG Oral Tablet — RxCUI 198365
RxNorm drug concept · Semantic clinical drug
RxCUI 198365
Semantic clinical drug · SCD
● Current RxNorm concept 47 FDA products
86 package NDCs
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI198365
Official nameProchlorperazine 10 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asprochlorperazine (as prochlorperazine maleate) 10 MG Oral Tablet; prochlorperazine maleate 10 MG Oral Tablet
FDA products mapped47
Package NDCs mapped86
Reported Medicaid activity (SDUD)218,717 prescriptions · 52 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Prochlorperazine: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Prochlorperazine is most commonly used to control severe nausea and vomiting. Depending on the form your doctor prescribed, it may also be used to treat schizophrenia. The tablet f...
- What is prochlorperazine actually used for?
- The most common ones are drowsiness, dizziness, blurred vision, and a drop in blood pressure when you stand up quickly. More serious — but less common — reactions include uncontrol...
- What side effects should I watch out for?
🕸️ Concept Web — How Prochlorperazine 10 MG Oral Tablet Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
Prochlorperazine 10 MG Oral Tablet
RxCUI 198365 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
-
Prochlorperazine
8704IN
-
Prochlorperazine
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Compazine
203546BN
-
Compazine
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Prochlorperazine Oral Tablet
373609SCDF -
Prochlorperazine Oral Product
1162280SCDG -
Prochlorperazine Pill
1162281SCDG -
Prochlorperazine Oral Tablet [Compazine]
368096SBDF -
Compazine Oral Product
1167412SBDG -
Compazine Pill
1167413SBDG -
Oral Tablet
317541DF -
Oral Product
1151131DFG - +1 more in this family
-
Prochlorperazine Oral Tablet
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Prochlorperazine 10 MG
316594SCDC -
Prochlorperazine 10 MG Oral Tablet [Compazine]
207685SBD -
Prochlorperazine 10 MG [Compazine]
568433SBDC
-
Prochlorperazine 10 MG
Showing up to 8 concepts per family — 13 of 14 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
-
Prochlorperazine 10 MG
SCDC · 316594 -
Prochlorperazine Oral Tablet
SCDF · 373609 -
Prochlorperazine Oral Product
SCDG · 1162280 -
Prochlorperazine Pill
SCDG · 1162281
Brand-Name Concepts
-
Prochlorperazine 10 MG Oral Tablet [Compazine]
SBD · 207685 -
Prochlorperazine 10 MG [Compazine]
SBDC · 568433 -
Prochlorperazine Oral Tablet [Compazine]
SBDF · 368096 -
Compazine Oral Product
SBDG · 1167412 -
Compazine Pill
SBDG · 1167413 -
Compazine
BN · 203546
📦 FDA Products & Package NDCs
47 products · 86 package NDCs
86 package NDCs map to RxCUI 198365 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 69452-0310-32 | 1000 TABLET, FILM COATED in 1 BOTTLE (69452-310-32) | PROCHLORPERAZINE MALEATE | Bionpharma Inc. | 2023-09-13 |
| 69452-0471-20 | 100 TABLET in 1 BOTTLE (69452-471-20) | PROCHLORPERAZINE MALEATE | Bionpharma Inc. | 2025-01-31 |
| 69452-0471-32 | 1000 TABLET in 1 BOTTLE (69452-471-32) | PROCHLORPERAZINE MALEATE | Bionpharma Inc. | 2025-01-31 |
| 69452-0472-20 | 100 TABLET in 1 BOTTLE (69452-472-20) | PROCHLORPERAZINE MALEATE | Bionpharma Inc. | 2025-01-31 |
| 69452-0472-32 | 1000 TABLET in 1 BOTTLE (69452-472-32) | PROCHLORPERAZINE MALEATE | Bionpharma Inc. | 2025-01-31 |
| 70518-4200-00 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-4200-0) | Prochlorperazine Maleate | REMEDYREPACK INC. | 2024-10-02 |
| 70518-4319-00 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-4319-0) | Prochlorperazine Maleate | REMEDYREPACK INC. | 2025-03-25 |
| 70710-1667-01 | 100 TABLET in 1 BOTTLE (70710-1667-1) | Prochlorperazine Maleate | Zydus Pharmaceuticals (USA) Inc. | 2022-08-10 |
| 70710-1668-01 | 100 TABLET in 1 BOTTLE (70710-1668-1) | Prochlorperazine Maleate | Zydus Pharmaceuticals (USA) Inc. | 2022-08-10 |
| 70771-1697-01 | 100 TABLET in 1 BOTTLE (70771-1697-1) | Prochlorperazine Maleate | Zydus Lifesciences Limited | 2022-08-10 |
| 70771-1698-01 | 100 TABLET in 1 BOTTLE (70771-1698-1) | Prochlorperazine Maleate | Zydus Lifesciences Limited | 2022-08-10 |
| 71335-0952-01 | 10 TABLET in 1 BOTTLE (71335-0952-1) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-0952-02 | 30 TABLET in 1 BOTTLE (71335-0952-2) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-0952-03 | 20 TABLET in 1 BOTTLE (71335-0952-3) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-0952-04 | 60 TABLET in 1 BOTTLE (71335-0952-4) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-0952-05 | 4 TABLET in 1 BOTTLE (71335-0952-5) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-0952-06 | 5 TABLET in 1 BOTTLE (71335-0952-6) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-0952-07 | 100 TABLET in 1 BOTTLE (71335-0952-7) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-0952-08 | 6 TABLET in 1 BOTTLE (71335-0952-8) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2006-03-14 |
| 71335-2386-01 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2386-1) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 71335-2386-02 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2386-2) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 71335-2386-03 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2386-3) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 71335-2386-04 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2386-4) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 71335-2386-05 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-2386-5) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 71335-2386-06 | 5 TABLET, FILM COATED in 1 BOTTLE (71335-2386-6) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 71335-2386-07 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2386-7) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 71335-2386-08 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-2386-8) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 2024-05-29 |
| 72162-2262-01 | 100 TABLET in 1 BOTTLE (72162-2262-1) | PROCHLORPERAZINE MALEATE | Bryant Ranch Prepack | 1998-03-01 |
| 72189-0503-30 | 30 TABLET in 1 BOTTLE (72189-503-30) | Prochlorperazine Maleate | Direct_Rx | 2023-08-03 |
| 72603-0169-01 | 100 TABLET in 1 BOTTLE (72603-169-01) | Prochlorperazine Maleate | Northstar Rx LLC | 2023-09-07 |
| 72789-0517-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-517-01) | PROCHLORPERAZINE MALEATE | PD-Rx Pharmaceuticals, Inc. | 2025-07-28 |
| 72789-0517-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-517-90) | PROCHLORPERAZINE MALEATE | PD-Rx Pharmaceuticals, Inc. | 2025-07-28 |
| 72789-0518-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-518-01) | PROCHLORPERAZINE MALEATE | PD-Rx Pharmaceuticals, Inc. | 2025-07-28 |
| 72789-0518-15 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-518-15) | PROCHLORPERAZINE MALEATE | PD-Rx Pharmaceuticals, Inc. | 2025-12-15 |
| 72789-0518-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-518-90) | PROCHLORPERAZINE MALEATE | PD-Rx Pharmaceuticals, Inc. | 2025-07-28 |
| 82868-0044-30 | 30 TABLET in 1 BOTTLE, PLASTIC (82868-044-30) | Prochlorperazine Maleate | Northwind Health Company, LLC | 2024-02-06 |
Observed labelers:
Bryant Ranch Prepack (17) ·
Bionpharma Inc. (8) ·
Proficient Rx LP (8) ·
PD-Rx Pharmaceuticals, Inc. (7) ·
Preferred Pharmaceuticals Inc. (5) ·
Amneal Pharmaceuticals NY LLC (4)
· +19 more — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.