prochlorperazine maleate
Generic: prochlorperazine maleate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
prochlorperazine maleate
Generic Name
prochlorperazine maleate
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
prochlorperazine maleate 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7634
Product ID
50090-7634_2e73b418-e83e-42be-af6b-293f0f7873da
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217478
Listing Expiration
2026-12-31
Marketing Start
2025-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907634
Hyphenated Format
50090-7634
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 6 TABLET in 1 BOTTLE (50090-7634-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e73b418-e83e-42be-af6b-293f0f7873da", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["f387b07a-2d99-4fd5-bcd1-8f04e69b8a39"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (50090-7634-5)", "package_ndc": "50090-7634-5", "marketing_start_date": "20250818"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "50090-7634_2e73b418-e83e-42be-af6b-293f0f7873da", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50090-7634", "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": "20250131", "listing_expiration_date": "20261231"}