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 70518-3106
Product ID 70518-3106_3a10a2f8-509a-97d9-e063-6394a90abe8f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040226
Listing Expiration 2026-12-31
Marketing Start 2021-05-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183106
Hyphenated Format 70518-3106

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
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3106-0)
source: ndc

Packages (1)

70518-3106-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3106-0)

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": "3a10a2f8-509a-97d9-e063-6394a90abe8f", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198077"], "spl_set_id": ["4ee52e79-6e3a-4b97-8c27-4f1b5dedd4a4"], "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 (70518-3106-0)", "package_ndc": "70518-3106-0", "marketing_start_date": "20210526"}], "brand_name": "Perphenazine", "product_id": "70518-3106_3a10a2f8-509a-97d9-e063-6394a90abe8f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3106", "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": "ANDA040226", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}