fluphenazine hydrochloride
Generic: fluphenazine hydrochloride
Labeler: amneal pharmaceuticals ny llcDrug Facts
Product Profile
Brand Name
fluphenazine hydrochloride
Generic Name
fluphenazine hydrochloride
Labeler
amneal pharmaceuticals ny llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
fluphenazine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69238-1680
Product ID
69238-1680_47a90e7b-4fe1-47a7-a427-de52037fb30b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213647
Listing Expiration
2026-12-31
Marketing Start
2020-07-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
692381680
Hyphenated Format
69238-1680
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
fluphenazine hydrochloride (source: ndc)
Generic Name
fluphenazine hydrochloride (source: ndc)
Application Number
ANDA213647 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1680-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47a90e7b-4fe1-47a7-a427-de52037fb30b", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["5b443b30-5682-4cf3-9ed0-716efddbc865"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1680-1)", "package_ndc": "69238-1680-1", "marketing_start_date": "20200711"}], "brand_name": "fluphenazine hydrochloride", "product_id": "69238-1680_47a90e7b-4fe1-47a7-a427-de52037fb30b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "69238-1680", "generic_name": "fluphenazine hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluphenazine hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA213647", "marketing_category": "ANDA", "marketing_start_date": "20200711", "listing_expiration_date": "20261231"}