fluphenazine decanoate
Generic: fluphenazine decanoate
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
fluphenazine decanoate
Generic Name
fluphenazine decanoate
Labeler
endo usa, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
fluphenazine decanoate 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
42023-129
Product ID
42023-129_088a5d84-ec79-4e0e-96b1-29e31e6aa39f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203732
Listing Expiration
2026-12-31
Marketing Start
2014-07-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42023129
Hyphenated Format
42023-129
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 decanoate (source: ndc)
Generic Name
fluphenazine decanoate (source: ndc)
Application Number
ANDA203732 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 1 VIAL in 1 CARTON (42023-129-01) / 5 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "SUBCUTANEOUS"], "spl_id": "088a5d84-ec79-4e0e-96b1-29e31e6aa39f", "openfda": {"unii": ["FMU62K1L3C"], "rxcui": ["859824"], "spl_set_id": ["b580471f-44a1-4da0-96ad-2f537eabec3e"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42023-129-01) / 5 mL in 1 VIAL", "package_ndc": "42023-129-01", "marketing_start_date": "20140709"}], "brand_name": "Fluphenazine Decanoate", "product_id": "42023-129_088a5d84-ec79-4e0e-96b1-29e31e6aa39f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "42023-129", "generic_name": "Fluphenazine Decanoate", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Decanoate", "active_ingredients": [{"name": "FLUPHENAZINE DECANOATE", "strength": "25 mg/mL"}], "application_number": "ANDA203732", "marketing_category": "ANDA", "marketing_start_date": "20140709", "listing_expiration_date": "20261231"}