prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prochlorperazine maleate 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-502
Product ID 63187-502_ba21a8c5-5ab9-4c89-921c-347a068240bc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040268
Listing Expiration 2026-12-31
Marketing Start 1998-03-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187502
Hyphenated Format 63187-502

Supplemental Identifiers

RxCUI
198365 312635
UPC
0363187251901 0363187502904
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
  • 5 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (63187-502-15)
  • 30 TABLET in 1 BOTTLE (63187-502-30)
  • 60 TABLET in 1 BOTTLE (63187-502-60)
  • 90 TABLET in 1 BOTTLE (63187-502-90)
source: ndc

Packages (4)

Ingredients (1)

prochlorperazine maleate (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ba21a8c5-5ab9-4c89-921c-347a068240bc", "openfda": {"upc": ["0363187251901", "0363187502904"], "unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["565e4b1b-04be-47b4-99b0-903fc2ed47af"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (63187-502-15)", "package_ndc": "63187-502-15", "marketing_start_date": "20181201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-502-30)", "package_ndc": "63187-502-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-502-60)", "package_ndc": "63187-502-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-502-90)", "package_ndc": "63187-502-90", "marketing_start_date": "20181201"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "63187-502_ba21a8c5-5ab9-4c89-921c-347a068240bc", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "63187-502", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "19980301", "listing_expiration_date": "20261231"}