perphenazine

Generic: perphenazine

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name perphenazine
Generic Name perphenazine
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

perphenazine 8 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-801
Product ID 23155-801_4cc7f39f-fa21-4dc0-8ff7-5d6e5a7236a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210163
Listing Expiration 2026-12-31
Marketing Start 2022-07-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155801
Hyphenated Format 23155-801

Supplemental Identifiers

RxCUI
198075 198076 198077 198078
UPC
0323155800012
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 ANDA210163 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-801-01)
source: ndc

Packages (1)

Ingredients (1)

perphenazine (8 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4cc7f39f-fa21-4dc0-8ff7-5d6e5a7236a2", "openfda": {"nui": ["N0000175746", "M0016525"], "upc": ["0323155800012"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075", "198076", "198077", "198078"], "spl_set_id": ["935a7567-0395-4901-960c-79587fa14c8d"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-801-01)", "package_ndc": "23155-801-01", "marketing_start_date": "20221001"}], "brand_name": "PERPHENAZINE", "product_id": "23155-801_4cc7f39f-fa21-4dc0-8ff7-5d6e5a7236a2", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "23155-801", "generic_name": "PERPHENAZINE", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PERPHENAZINE", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "8 mg/1"}], "application_number": "ANDA210163", "marketing_category": "ANDA", "marketing_start_date": "20220710", "listing_expiration_date": "20261231"}