prochlorperazine maleate
Generic: prochlorperazine maleate
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
prochlorperazine maleate
Generic Name
prochlorperazine maleate
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
prochlorperazine maleate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82868-044
Product ID
82868-044_47a70b0b-9e78-e333-e063-6394a90a6bd2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216495
Listing Expiration
2027-12-31
Marketing Start
2024-02-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82868044
Hyphenated Format
82868-044
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
ANDA216495 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (82868-044-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47a70b0b-9e78-e333-e063-6394a90a6bd2", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["115a4125-07df-9f9b-e063-6394a90a3e49"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-044-30)", "package_ndc": "82868-044-30", "marketing_start_date": "20240206"}], "brand_name": "Prochlorperazine Maleate", "product_id": "82868-044_47a70b0b-9e78-e333-e063-6394a90a6bd2", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "82868-044", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA216495", "marketing_category": "ANDA", "marketing_start_date": "20240206", "listing_expiration_date": "20271231"}