perphenazine

Generic: perphenazine

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

Drug Facts

Product Profile

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

perphenazine 2 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 0603-5060
Product ID 0603-5060_984ac2cf-c025-44e1-b1bb-a73260473881
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040226
Listing Expiration 2026-12-31
Marketing Start 1998-12-31

Pharmacologic Class

Established (EPC)
phenothiazine [epc]
Chemical Structure
phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06035060
Hyphenated Format 0603-5060

Supplemental Identifiers

RxCUI
198075 198076 198077 198078
UNII
FTA7XXY4EZ
NUI
N0000175746 M0016525

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 perphenazine (source: ndc)
Generic Name perphenazine (source: ndc)
Application Number ANDA040226 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-5060-21)
source: ndc

Packages (1)

Ingredients (1)

perphenazine (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "984ac2cf-c025-44e1-b1bb-a73260473881", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075", "198076", "198077", "198078"], "spl_set_id": ["5fbfe9da-26e8-4705-98f3-42acd3d7b439"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-5060-21)", "package_ndc": "0603-5060-21", "marketing_start_date": "19981231"}], "brand_name": "Perphenazine", "product_id": "0603-5060_984ac2cf-c025-44e1-b1bb-a73260473881", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0603-5060", "generic_name": "perphenazine", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "2 mg/1"}], "application_number": "ANDA040226", "marketing_category": "ANDA", "marketing_start_date": "19981231", "listing_expiration_date": "20261231"}