prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

prochlorperazine maleate 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7147
Product ID 50090-7147_8b09b8d5-0219-4106-8268-94d0bdbff394
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217478
Listing Expiration 2026-12-31
Marketing Start 2023-09-13

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907147
Hyphenated Format 50090-7147

Supplemental Identifiers

RxCUI
312635
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 ANDA217478 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 3 TABLET, FILM COATED in 1 BOTTLE (50090-7147-0)
  • 6 TABLET, FILM COATED in 1 BOTTLE (50090-7147-5)
source: ndc

Packages (2)

50090-7147-0 3 TABLET, FILM COATED in 1 BOTTLE (50090-7147-0) 50090-7147-5 6 TABLET, FILM COATED in 1 BOTTLE (50090-7147-5)

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": "8b09b8d5-0219-4106-8268-94d0bdbff394", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["86102abe-0b72-4352-95ce-db88d2e14002"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (50090-7147-0)", "package_ndc": "50090-7147-0", "marketing_start_date": "20240426"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50090-7147-5)", "package_ndc": "50090-7147-5", "marketing_start_date": "20240501"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "50090-7147_8b09b8d5-0219-4106-8268-94d0bdbff394", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50090-7147", "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": "ANDA217478", "marketing_category": "ANDA", "marketing_start_date": "20230913", "listing_expiration_date": "20261231"}