prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-774
Product ID 59651-774_7ec4df20-9ea5-4a68-a43f-5ded4eaed235
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218734
Listing Expiration 2026-12-31
Marketing Start 2025-09-08

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651774
Hyphenated Format 59651-774

Supplemental Identifiers

RxCUI
198365 312635
UNII
I1T8O1JTL6

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name prochlorperazine maleate (source: ndc)
Generic Name prochlorperazine maleate (source: ndc)
Application Number ANDA218734 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59651-774-01)
source: ndc

Packages (1)

59651-774-01 100 TABLET, FILM COATED in 1 BOTTLE (59651-774-01)

Ingredients (1)

prochlorperazine maleate (10 mg/1)

Linked Drug Pages (1)

prochlorperazine maleate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7ec4df20-9ea5-4a68-a43f-5ded4eaed235", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["7ec4df20-9ea5-4a68-a43f-5ded4eaed235"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-774-01)", "package_ndc": "59651-774-01", "marketing_start_date": "20250908"}], "brand_name": "prochlorperazine maleate", "product_id": "59651-774_7ec4df20-9ea5-4a68-a43f-5ded4eaed235", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "59651-774", "generic_name": "prochlorperazine maleate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prochlorperazine maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA218734", "marketing_category": "ANDA", "marketing_start_date": "20250908", "listing_expiration_date": "20261231"}