perphenazine

Generic: perphenazine

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name perphenazine
Generic Name perphenazine
Labeler major pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

perphenazine 4 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6600
Product ID 0904-6600_d6aac7df-10a5-4fe2-ad3a-882af0077f16
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 09046600
Hyphenated Format 0904-6600

Supplemental Identifiers

RxCUI
198076 198077 198078
UNII
FTA7XXY4EZ
NUI
N0000175746 M0016525

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
  • 4 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6600-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6600-61 100 BLISTER PACK in 1 CARTON (0904-6600-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

perphenazine (4 mg/1)

Linked Drug Pages (1)

Perphenazine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d6aac7df-10a5-4fe2-ad3a-882af0077f16", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198076", "198077", "198078"], "spl_set_id": ["0dc77ea9-32ee-4b6d-b69d-8c712bcf5fe4"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6600-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6600-61", "marketing_start_date": "19981231"}], "brand_name": "Perphenazine", "product_id": "0904-6600_d6aac7df-10a5-4fe2-ad3a-882af0077f16", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0904-6600", "generic_name": "perphenazine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "4 mg/1"}], "application_number": "ANDA040226", "marketing_category": "ANDA", "marketing_start_date": "19981231", "listing_expiration_date": "20261231"}