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
Routes
ORAL
Active Ingredients

perphenazine 2 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3257
Product ID 70518-3257_3a38572a-6805-90f5-e063-6394a90a9b93
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205232
Listing Expiration 2026-12-31
Marketing Start 2021-10-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183257
Hyphenated Format 70518-3257

Supplemental Identifiers

RxCUI
198076
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 ANDA205232 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-3257-0)
source: ndc

Packages (1)

70518-3257-0 30 TABLET in 1 BLISTER PACK (70518-3257-0)

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": "3a38572a-6805-90f5-e063-6394a90a9b93", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198076"], "spl_set_id": ["1fc98e41-17d1-4491-87ed-ff7651422b5b"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3257-0)", "package_ndc": "70518-3257-0", "marketing_start_date": "20211027"}], "brand_name": "perphenazine", "product_id": "70518-3257_3a38572a-6805-90f5-e063-6394a90a9b93", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3257", "generic_name": "perphenazine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "2 mg/1"}], "application_number": "ANDA205232", "marketing_category": "ANDA", "marketing_start_date": "20211027", "listing_expiration_date": "20261231"}