perphenazine

Generic: perphenazine

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name perphenazine
Generic Name perphenazine
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

perphenazine 8 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1043
Product ID 70771-1043_e7ec4ac9-7976-4574-9837-56b48606144b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205232
Listing Expiration 2026-12-31
Marketing Start 2020-07-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711043
Hyphenated Format 70771-1043

Supplemental Identifiers

RxCUI
198075 198076 198077 198078
UPC
0370771104215 0370771104116
UNII
FTA7XXY4EZ
NUI
N0000175746 M0016525

Packaging Origin

Original Packager
true

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
  • 8 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70771-1043-1)
  • 10 BLISTER PACK in 1 CARTON (70771-1043-4) / 10 TABLET in 1 BLISTER PACK (70771-1043-2)
  • 500 TABLET in 1 BOTTLE (70771-1043-5)
source: ndc

Packages (3)

70771-1043-1 100 TABLET in 1 BOTTLE (70771-1043-1) 70771-1043-4 10 BLISTER PACK in 1 CARTON (70771-1043-4) / 10 TABLET in 1 BLISTER PACK (70771-1043-2) 70771-1043-5 500 TABLET in 1 BOTTLE (70771-1043-5)

Ingredients (1)

perphenazine (8 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": "e7ec4ac9-7976-4574-9837-56b48606144b", "openfda": {"nui": ["N0000175746", "M0016525"], "upc": ["0370771104215", "0370771104116"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075", "198076", "198077", "198078"], "spl_set_id": ["003fe32c-a55d-4191-99fa-1013522b1b2e"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1043-1)", "package_ndc": "70771-1043-1", "marketing_start_date": "20200716"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1043-4)  / 10 TABLET in 1 BLISTER PACK (70771-1043-2)", "package_ndc": "70771-1043-4", "marketing_start_date": "20200716"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1043-5)", "package_ndc": "70771-1043-5", "marketing_start_date": "20200716"}], "brand_name": "perphenazine", "product_id": "70771-1043_e7ec4ac9-7976-4574-9837-56b48606144b", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70771-1043", "generic_name": "perphenazine", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "8 mg/1"}], "application_number": "ANDA205232", "marketing_category": "ANDA", "marketing_start_date": "20200716", "listing_expiration_date": "20261231"}