prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-503
Product ID 72189-503_2c4e4a5c-f12a-8c46-e063-6394a90ae95e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040268
Listing Expiration 2026-12-31
Marketing Start 2023-08-03

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189503
Hyphenated Format 72189-503

Supplemental Identifiers

RxCUI
198365
UNII
I1T8O1JTL6

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 ANDA040268 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-503-30)
source: ndc

Packages (1)

72189-503-30 30 TABLET in 1 BOTTLE (72189-503-30)

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": "2c4e4a5c-f12a-8c46-e063-6394a90ae95e", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["02069e43-5245-20dc-e063-6294a90a9dcd"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-503-30)", "package_ndc": "72189-503-30", "marketing_start_date": "20230803"}], "brand_name": "Prochlorperazine Maleate", "product_id": "72189-503_2c4e4a5c-f12a-8c46-e063-6394a90ae95e", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72189-503", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "20230803", "listing_expiration_date": "20261231"}