prochlorperazine

Generic: prochlorperazine

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

Drug Facts

Product Profile

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

prochlorperazine maleate 5 mg/1

Manufacturer
PharmPak, Inc.

Identifiers & Regulatory

Product NDC 54348-989
Product ID 54348-989_eaa6022b-bb02-9383-e053-2995a90abe88
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040268
Listing Expiration 2026-12-31
Marketing Start 2019-07-11

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 54348989
Hyphenated Format 54348-989

Supplemental Identifiers

RxCUI
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 (source: ndc)
Generic Name prochlorperazine (source: ndc)
Application Number ANDA040268 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 BOX (54348-989-06) / 6 TABLET in 1 BOTTLE
source: ndc

Packages (1)

54348-989-06 1 BOTTLE in 1 BOX (54348-989-06) / 6 TABLET in 1 BOTTLE

Ingredients (1)

prochlorperazine maleate (5 mg/1)

Linked Drug Pages (1)

Prochlorperazine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eaa6022b-bb02-9383-e053-2995a90abe88", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["383744db-ba57-478a-8041-2ecc26d3e1ec"], "manufacturer_name": ["PharmPak, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (54348-989-06)  / 6 TABLET in 1 BOTTLE", "package_ndc": "54348-989-06", "marketing_start_date": "20190711"}], "brand_name": "Prochlorperazine", "product_id": "54348-989_eaa6022b-bb02-9383-e053-2995a90abe88", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "54348-989", "generic_name": "PROCHLORPERAZINE", "labeler_name": "PharmPak, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "20190711", "listing_expiration_date": "20261231"}