prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-169
Product ID 72603-169_2dda6392-975a-4d77-e063-6294a90a2f67
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216202
Listing Expiration 2026-12-31
Marketing Start 2023-09-07

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603169
Hyphenated Format 72603-169

Supplemental Identifiers

RxCUI
198365 312635
UNII
I1T8O1JTL6

Packaging Origin

Original Packager
true

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
  • 100 TABLET in 1 BOTTLE (72603-169-01)
source: ndc

Packages (1)

Ingredients (1)

prochlorperazine maleate (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2dda6392-975a-4d77-e063-6294a90a2f67", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["04bf8a16-218a-c648-e063-6294a90a1afb"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-169-01)", "package_ndc": "72603-169-01", "marketing_start_date": "20230907"}], "brand_name": "Prochlorperazine Maleate", "product_id": "72603-169_2dda6392-975a-4d77-e063-6294a90a2f67", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72603-169", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Northstar Rx LLC", "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": "20230907", "listing_expiration_date": "20261231"}