perphenazine

Generic: perphenazine

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

perphenazine 2 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-8046
Product ID 0781-8046_9e348a80-ecb9-409b-91e7-3a48423314ff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089685
Marketing Start 1988-12-08
Marketing End 2027-03-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07818046
Hyphenated Format 0781-8046

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 ANDA089685 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0781-8046-01)
source: ndc

Packages (1)

0781-8046-01 100 TABLET, FILM COATED in 1 BOTTLE (0781-8046-01)

Ingredients (1)

perphenazine (2 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": "9e348a80-ecb9-409b-91e7-3a48423314ff", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075", "198076", "198077", "198078"], "spl_set_id": ["fc32500c-cc42-4f85-9cee-88f983fcbc16"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-8046-01)", "package_ndc": "0781-8046-01", "marketing_end_date": "20270321", "marketing_start_date": "20180828"}], "brand_name": "Perphenazine", "product_id": "0781-8046_9e348a80-ecb9-409b-91e7-3a48423314ff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0781-8046", "generic_name": "Perphenazine", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "2 mg/1"}], "application_number": "ANDA089685", "marketing_category": "ANDA", "marketing_end_date": "20270321", "marketing_start_date": "19881208"}