Perphenazine

Generic: Perphenazine

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Perphenazine
Generic Name Perphenazine
Labeler REMEDYREPACK INC.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

PERPHENAZINE 4 mg/1

Identifiers & Regulatory

Product NDC 70518-4112
Product ID 70518-4112_1bcdd8e4-c483-22ca-e063-6294a90af66a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089685
Marketing Start 2024-06-25
Marketing End 2027-03-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184112
Hyphenated Format 70518-4112

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
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4112-0)
source: ndc

Packages (1)

70518-4112-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4112-0)

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": "1bcdd8e4-c483-22ca-e063-6294a90af66a", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198077"], "spl_set_id": ["9588d223-41e4-4bb2-9306-f082498404c5"], "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 (70518-4112-0)", "package_ndc": "70518-4112-0", "marketing_end_date": "20270321", "marketing_start_date": "20240625"}], "brand_name": "Perphenazine", "product_id": "70518-4112_1bcdd8e4-c483-22ca-e063-6294a90af66a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4112", "generic_name": "Perphenazine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "4 mg/1"}], "application_number": "ANDA089685", "marketing_category": "ANDA", "marketing_end_date": "20270321", "marketing_start_date": "20240625"}