pimozide

Generic: pimozide

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

Drug Facts

Product Profile

Brand Name pimozide
Generic Name pimozide
Labeler endo usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pimozide 2 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 49884-348
Product ID 49884-348_2a1e4060-1340-49c7-86f9-9f4206124b3d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204521
Listing Expiration 2026-12-31
Marketing Start 2015-09-28

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49884348
Hyphenated Format 49884-348

Supplemental Identifiers

RxCUI
198103 312439
UPC
0349884348014 0349884347017
UNII
1HIZ4DL86F
NUI
N0000180182

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 pimozide (source: ndc)
Generic Name pimozide (source: ndc)
Application Number ANDA204521 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (49884-348-01)
source: ndc

Packages (1)

49884-348-01 100 TABLET in 1 BOTTLE (49884-348-01)

Ingredients (1)

pimozide (2 mg/1)

Linked Drug Pages (1)

Pimozide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a1e4060-1340-49c7-86f9-9f4206124b3d", "openfda": {"nui": ["N0000180182"], "upc": ["0349884348014", "0349884347017"], "unii": ["1HIZ4DL86F"], "rxcui": ["198103", "312439"], "spl_set_id": ["70b079e2-a1f7-4a93-8685-d60a4d7c1280"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49884-348-01)", "package_ndc": "49884-348-01", "marketing_start_date": "20150928"}], "brand_name": "Pimozide", "product_id": "49884-348_2a1e4060-1340-49c7-86f9-9f4206124b3d", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "49884-348", "generic_name": "Pimozide", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pimozide", "active_ingredients": [{"name": "PIMOZIDE", "strength": "2 mg/1"}], "application_number": "ANDA204521", "marketing_category": "ANDA", "marketing_start_date": "20150928", "listing_expiration_date": "20261231"}