prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

prochlorperazine maleate 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2621
Product ID 71335-2621_9002b9dd-0012-4f2e-8770-3e8a8ef463f9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217478
Listing Expiration 2026-12-31
Marketing Start 2023-09-13

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352621
Hyphenated Format 71335-2621

Supplemental Identifiers

RxCUI
312635
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
  • 5 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (71335-2621-1)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71335-2621-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-2621-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-2621-4)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-2621-5)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-2621-6)
  • 6 TABLET, FILM COATED in 1 BOTTLE (71335-2621-7)
source: ndc

Packages (7)

71335-2621-1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2621-1) 71335-2621-2 10 TABLET, FILM COATED in 1 BOTTLE (71335-2621-2) 71335-2621-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-2621-3) 71335-2621-4 60 TABLET, FILM COATED in 1 BOTTLE (71335-2621-4) 71335-2621-5 90 TABLET, FILM COATED in 1 BOTTLE (71335-2621-5) 71335-2621-6 120 TABLET, FILM COATED in 1 BOTTLE (71335-2621-6) 71335-2621-7 6 TABLET, FILM COATED in 1 BOTTLE (71335-2621-7)

Ingredients (1)

prochlorperazine maleate (5 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": "9002b9dd-0012-4f2e-8770-3e8a8ef463f9", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["3ccd11d3-5e5e-4ed8-9b0c-49b0a84535ab"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2621-1)", "package_ndc": "71335-2621-1", "marketing_start_date": "20250324"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-2621-2)", "package_ndc": "71335-2621-2", "marketing_start_date": "20250324"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2621-3)", "package_ndc": "71335-2621-3", "marketing_start_date": "20250324"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2621-4)", "package_ndc": "71335-2621-4", "marketing_start_date": "20250324"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2621-5)", "package_ndc": "71335-2621-5", "marketing_start_date": "20250324"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2621-6)", "package_ndc": "71335-2621-6", "marketing_start_date": "20250324"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71335-2621-7)", "package_ndc": "71335-2621-7", "marketing_start_date": "20250324"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "71335-2621_9002b9dd-0012-4f2e-8770-3e8a8ef463f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "71335-2621", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA217478", "marketing_category": "ANDA", "marketing_start_date": "20230913", "listing_expiration_date": "20261231"}