perphenazine

Generic: perphenazine

Labeler: zydus pharmaceuticals (usa) inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name perphenazine
Generic Name perphenazine
Labeler zydus pharmaceuticals (usa) inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

perphenazine 8 mg/1

Manufacturer
Zydus Pharmaceuticals (USA) Inc.

Identifiers & Regulatory

Product NDC 68382-593
Product ID 68382-593_520360a9-ddcd-46f4-995b-d776c5b2937c
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 68382593
Hyphenated Format 68382-593

Supplemental Identifiers

RxCUI
198075 198076 198077 198078
UPC
0368382591012
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 (68382-593-01)
  • 500 TABLET in 1 BOTTLE (68382-593-05)
  • 10 BLISTER PACK in 1 CARTON (68382-593-30) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (3)

68382-593-01 100 TABLET in 1 BOTTLE (68382-593-01) 68382-593-05 500 TABLET in 1 BOTTLE (68382-593-05) 68382-593-30 10 BLISTER PACK in 1 CARTON (68382-593-30) / 10 TABLET in 1 BLISTER PACK

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": "520360a9-ddcd-46f4-995b-d776c5b2937c", "openfda": {"nui": ["N0000175746", "M0016525"], "upc": ["0368382591012"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075", "198076", "198077", "198078"], "spl_set_id": ["c209f1f6-f440-4366-8140-1d24cf0c2ce6"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-593-01)", "package_ndc": "68382-593-01", "marketing_start_date": "20200716"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-593-05)", "package_ndc": "68382-593-05", "marketing_start_date": "20200716"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-593-30)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "68382-593-30", "marketing_start_date": "20200716"}], "brand_name": "perphenazine", "product_id": "68382-593_520360a9-ddcd-46f4-995b-d776c5b2937c", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68382-593", "generic_name": "perphenazine", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "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"}