prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

prochlorperazine maleate 5 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-814
Product ID 60687-814_1b333ecf-b60b-8af8-e063-6394a90af538
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216598
Listing Expiration 2026-12-31
Marketing Start 2024-09-15

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687814
Hyphenated Format 60687-814

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 ANDA216598 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 CARTON (60687-814-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-814-11)
source: ndc

Packages (1)

60687-814-65 50 BLISTER PACK in 1 CARTON (60687-814-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-814-11)

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": "1b333ecf-b60b-8af8-e063-6394a90af538", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["459fbfd6-f6fe-4589-894f-acd69b413de6"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-814-65)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-814-11)", "package_ndc": "60687-814-65", "marketing_start_date": "20240915"}], "brand_name": "Prochlorperazine Maleate", "product_id": "60687-814_1b333ecf-b60b-8af8-e063-6394a90af538", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "60687-814", "generic_name": "Prochlorperazine Maleate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA216598", "marketing_category": "ANDA", "marketing_start_date": "20240915", "listing_expiration_date": "20261231"}