prochlorperazine maleate

Generic: prochlorperazine maleate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-742
Product ID 43063-742_2b37cf4b-b873-1752-e063-6394a90a40b6
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 43063742
Hyphenated Format 43063-742

Supplemental Identifiers

RxCUI
198365
UPC
0343063742150
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
  • 6 TABLET in 1 BOTTLE, PLASTIC (43063-742-06)
  • 15 TABLET in 1 BOTTLE, PLASTIC (43063-742-15)
source: ndc

Packages (2)

43063-742-06 6 TABLET in 1 BOTTLE, PLASTIC (43063-742-06) 43063-742-15 15 TABLET in 1 BOTTLE, PLASTIC (43063-742-15)

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": "2b37cf4b-b873-1752-e063-6394a90a40b6", "openfda": {"upc": ["0343063742150"], "unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["fc77a504-4642-47c1-b2e3-c5db11e5816d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (43063-742-06)", "package_ndc": "43063-742-06", "marketing_start_date": "20170206"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (43063-742-15)", "package_ndc": "43063-742-15", "marketing_start_date": "20181108"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "43063-742_2b37cf4b-b873-1752-e063-6394a90a40b6", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43063-742", "generic_name": "Prochlorperazine maleate", "labeler_name": "PD-Rx Pharmaceuticals, 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"}