prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: qpharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler qpharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
QPharma, Inc.

Identifiers & Regulatory

Product NDC 42708-103
Product ID 42708-103_4682c28f-fee2-11c4-e063-6294a90a2342
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040268
Listing Expiration 2026-12-31
Marketing Start 1998-03-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42708103
Hyphenated Format 42708-103

Supplemental Identifiers

RxCUI
198365
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 ANDA040268 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE (42708-103-12)
source: ndc

Packages (1)

42708-103-12 12 TABLET in 1 BOTTLE (42708-103-12)

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": "4682c28f-fee2-11c4-e063-6294a90a2342", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["dc692e77-5240-4aa6-8fe9-9ffcbb267261"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "12 TABLET in 1 BOTTLE (42708-103-12)", "package_ndc": "42708-103-12", "marketing_start_date": "20191018"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "42708-103_4682c28f-fee2-11c4-e063-6294a90a2342", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "42708-103", "generic_name": "Prochlorperazine maleate", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "19980301", "listing_expiration_date": "20261231"}