prochlorperazine maleate
Generic: prochlorperazine maleate
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
prochlorperazine maleate
Generic Name
prochlorperazine maleate
Labeler
northstar rx llc
Dosage Form
TABLET
Routes
Active Ingredients
prochlorperazine maleate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72603-169
Product ID
72603-169_2dda6392-975a-4d77-e063-6294a90a2f67
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216202
Listing Expiration
2026-12-31
Marketing Start
2023-09-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72603169
Hyphenated Format
72603-169
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
ANDA216202 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (72603-169-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2dda6392-975a-4d77-e063-6294a90a2f67", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["04bf8a16-218a-c648-e063-6294a90a1afb"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-169-01)", "package_ndc": "72603-169-01", "marketing_start_date": "20230907"}], "brand_name": "Prochlorperazine Maleate", "product_id": "72603-169_2dda6392-975a-4d77-e063-6294a90a2f67", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72603-169", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA216202", "marketing_category": "ANDA", "marketing_start_date": "20230907", "listing_expiration_date": "20261231"}