perphenazine
Generic: perphenazine
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
perphenazine
Generic Name
perphenazine
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
perphenazine 8 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3108
Product ID
70518-3108_16d721f1-cbde-8ef8-e063-6394a90a7b41
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089685
Marketing Start
2021-05-28
Marketing End
2027-03-21
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183108
Hyphenated Format
70518-3108
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 8 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3108-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "16d721f1-cbde-8ef8-e063-6394a90a7b41", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198078"], "spl_set_id": ["fc903628-248c-4d12-88b4-a551aeadb4d2"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3108-0)", "package_ndc": "70518-3108-0", "marketing_end_date": "20270321", "marketing_start_date": "20210528"}], "brand_name": "Perphenazine", "product_id": "70518-3108_16d721f1-cbde-8ef8-e063-6394a90a7b41", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3108", "generic_name": "Perphenazine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "8 mg/1"}], "application_number": "ANDA089685", "marketing_category": "ANDA", "marketing_end_date": "20270321", "marketing_start_date": "20210528"}