PROCHLORPERAZINE MALEATE

Generic: Prochlorperazine Maleate

Labeler: A-S Medication Solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name PROCHLORPERAZINE MALEATE
Generic Name Prochlorperazine Maleate
Labeler A-S Medication Solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

PROCHLORPERAZINE MALEATE 5 mg/1

Identifiers & Regulatory

Product NDC 50090-2241
Product ID 50090-2241_e4c9234d-ba6e-4193-809b-21a57677302c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040268
Listing Expiration 2026-12-31
Marketing Start 1998-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902241
Hyphenated Format 50090-2241

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
  • 3 TABLET in 1 BOTTLE (50090-2241-0)
  • 6 TABLET in 1 BOTTLE (50090-2241-5)
source: ndc

Packages (2)

50090-2241-0 3 TABLET in 1 BOTTLE (50090-2241-0) 50090-2241-5 6 TABLET in 1 BOTTLE (50090-2241-5)

Ingredients (1)

PROCHLORPERAZINE MALEATE (5 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": "e4c9234d-ba6e-4193-809b-21a57677302c", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["8b58b63c-0a75-406b-bb29-acf0a40353bd"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET in 1 BOTTLE (50090-2241-0)", "package_ndc": "50090-2241-0", "marketing_start_date": "20181011"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (50090-2241-5)", "package_ndc": "50090-2241-5", "marketing_start_date": "20151124"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "50090-2241_e4c9234d-ba6e-4193-809b-21a57677302c", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50090-2241", "generic_name": "Prochlorperazine Maleate", "labeler_name": "A-S Medication Solutions", "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"}