perphenazine

Generic: perphenazine

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

perphenazine 8 mg/1

Manufacturer
REMEDYREPACK INC.

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)
phenothiazine [epc]
Chemical Structure
phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183108
Hyphenated Format 70518-3108

Supplemental Identifiers

RxCUI
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 ANDA089685 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3108-0)
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": "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"}