prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8708
Product ID 68788-8708_24979c05-5f42-4c42-b356-6069c2b46f8a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217478
Listing Expiration 2026-12-31
Marketing Start 2024-07-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888708
Hyphenated Format 68788-8708

Supplemental Identifiers

RxCUI
198365
UNII
I1T8O1JTL6

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (68788-8708-1)
  • 20 TABLET, FILM COATED in 1 BOTTLE (68788-8708-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-8708-3)
  • 15 TABLET, FILM COATED in 1 BOTTLE (68788-8708-5)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-8708-6)
source: ndc

Packages (5)

68788-8708-1 10 TABLET, FILM COATED in 1 BOTTLE (68788-8708-1) 68788-8708-2 20 TABLET, FILM COATED in 1 BOTTLE (68788-8708-2) 68788-8708-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-8708-3) 68788-8708-5 15 TABLET, FILM COATED in 1 BOTTLE (68788-8708-5) 68788-8708-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-8708-6)

Ingredients (1)

prochlorperazine maleate (10 mg/1)

Linked Drug Pages (1)

PROCHLORPERAZINE MALEATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24979c05-5f42-4c42-b356-6069c2b46f8a", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["f3adc8a4-2c2b-4d5e-803f-38361966cc68"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68788-8708-1)", "package_ndc": "68788-8708-1", "marketing_start_date": "20240701"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8708-2)", "package_ndc": "68788-8708-2", "marketing_start_date": "20240701"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8708-3)", "package_ndc": "68788-8708-3", "marketing_start_date": "20240701"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68788-8708-5)", "package_ndc": "68788-8708-5", "marketing_start_date": "20240701"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8708-6)", "package_ndc": "68788-8708-6", "marketing_start_date": "20240701"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "68788-8708_24979c05-5f42-4c42-b356-6069c2b46f8a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68788-8708", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA217478", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}