fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 10 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-419
Product ID 62135-419_458c6457-ed15-15f4-e063-6294a90acc6d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215141
Listing Expiration 2026-12-31
Marketing Start 2022-01-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135419
Hyphenated Format 62135-419

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0362135416904 0362135418908 0362135419905 0362135415907
UNII
ZOU145W1XL

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 fluphenazine hydrochloride (source: ndc)
Generic Name fluphenazine hydrochloride (source: ndc)
Application Number ANDA215141 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (62135-419-90)
source: ndc

Packages (1)

62135-419-90 90 TABLET, FILM COATED in 1 BOTTLE (62135-419-90)

Ingredients (1)

fluphenazine hydrochloride (10 mg/1)

Linked Drug Pages (1)

fluphenazine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "458c6457-ed15-15f4-e063-6294a90acc6d", "openfda": {"upc": ["0362135416904", "0362135418908", "0362135419905", "0362135415907"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["325af2a4-2280-4236-8cf8-44f5700ba73f"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-419-90)", "package_ndc": "62135-419-90", "marketing_start_date": "20221020"}], "brand_name": "fluphenazine hydrochloride", "product_id": "62135-419_458c6457-ed15-15f4-e063-6294a90acc6d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62135-419", "generic_name": "fluphenazine hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluphenazine hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA215141", "marketing_category": "ANDA", "marketing_start_date": "20220101", "listing_expiration_date": "20261231"}