prochlorperazine maleate
Generic: prochlorperazine maleate
Labeler: amneal pharmaceuticals ny llcDrug Facts
Product Profile
Brand Name
prochlorperazine maleate
Generic Name
prochlorperazine maleate
Labeler
amneal pharmaceuticals ny llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
prochlorperazine maleate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60219-2039
Product ID
60219-2039_1ecda8a1-7680-41a0-8b4f-00c3c4ef9b14
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216598
Listing Expiration
2026-12-31
Marketing Start
2023-04-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
602192039
Hyphenated Format
60219-2039
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA216598 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-1)
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-7)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ecda8a1-7680-41a0-8b4f-00c3c4ef9b14", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["a2a48790-0634-4b46-b362-98b7c252836f"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-1)", "package_ndc": "60219-2039-1", "marketing_start_date": "20230421"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-7)", "package_ndc": "60219-2039-7", "marketing_start_date": "20230421"}], "brand_name": "prochlorperazine maleate", "product_id": "60219-2039_1ecda8a1-7680-41a0-8b4f-00c3c4ef9b14", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "60219-2039", "generic_name": "prochlorperazine maleate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prochlorperazine maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA216598", "marketing_category": "ANDA", "marketing_start_date": "20230421", "listing_expiration_date": "20261231"}