prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7382
Product ID 0904-7382_8293831f-a230-4ae6-8e93-be496e20b7e7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216202
Listing Expiration 2026-12-31
Marketing Start 2022-08-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047382
Hyphenated Format 0904-7382

Supplemental Identifiers

RxCUI
198365 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 ANDA216202 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 CARTON (0904-7382-06) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7382-06 50 BLISTER PACK in 1 CARTON (0904-7382-06) / 1 TABLET in 1 BLISTER PACK

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": "8293831f-a230-4ae6-8e93-be496e20b7e7", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["d6fc83ad-9cce-4e60-854c-3825313ee60c"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7382-06)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7382-06", "marketing_start_date": "20231030"}], "brand_name": "Prochlorperazine Maleate", "product_id": "0904-7382_8293831f-a230-4ae6-8e93-be496e20b7e7", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0904-7382", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Major Pharmaceuticals", "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": "20220801", "listing_expiration_date": "20261231"}