prochlorperazine maleate
Generic: prochlorperazine maleate
Labeler: zydus pharmaceuticals (usa) inc.Drug Facts
Product Profile
Brand Name
prochlorperazine maleate
Generic Name
prochlorperazine maleate
Labeler
zydus pharmaceuticals (usa) inc.
Dosage Form
TABLET
Routes
Active Ingredients
prochlorperazine maleate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70710-1668
Product ID
70710-1668_da187256-50af-400b-ab27-a073f3fbe81a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216495
Listing Expiration
2026-12-31
Marketing Start
2022-08-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707101668
Hyphenated Format
70710-1668
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
ANDA216495 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (70710-1668-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "da187256-50af-400b-ab27-a073f3fbe81a", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["d4a34138-a01b-418f-8e0f-e81f6e1cfd89"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1668-1)", "package_ndc": "70710-1668-1", "marketing_start_date": "20220810"}], "brand_name": "Prochlorperazine Maleate", "product_id": "70710-1668_da187256-50af-400b-ab27-a073f3fbe81a", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1668", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "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": "20220810", "listing_expiration_date": "20261231"}