prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler redpharm drug
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

prochlorperazine maleate 5 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2099
Product ID 67296-2099_32519f04-c7b4-c09f-e063-6394a90aba84
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 672962099
Hyphenated Format 67296-2099

Supplemental Identifiers

RxCUI
312635
UPC
0369452309209 0369452310205
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
  • 15 TABLET, FILM COATED in 1 BOTTLE (67296-2099-1)
  • 10 TABLET, FILM COATED in 1 BOTTLE (67296-2099-9)
source: ndc

Packages (2)

67296-2099-1 15 TABLET, FILM COATED in 1 BOTTLE (67296-2099-1) 67296-2099-9 10 TABLET, FILM COATED in 1 BOTTLE (67296-2099-9)

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": "32519f04-c7b4-c09f-e063-6394a90aba84", "openfda": {"upc": ["0369452309209", "0369452310205"], "unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["18988af8-545a-3b69-e063-6394a90ae074"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (67296-2099-1)", "package_ndc": "67296-2099-1", "marketing_start_date": "20230913"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (67296-2099-9)", "package_ndc": "67296-2099-9", "marketing_start_date": "20230913"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "67296-2099_32519f04-c7b4-c09f-e063-6394a90aba84", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67296-2099", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Redpharm Drug", "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"}