fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: upsher-smith laboratories,llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler upsher-smith laboratories,llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 10 mg/1

Manufacturer
Upsher-Smith Laboratories,LLC

Identifiers & Regulatory

Product NDC 0832-6006
Product ID 0832-6006_3bb74f82-8872-9829-e063-6294a90aeace
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213784
Marketing Start 2022-11-22
Marketing End 2027-07-31

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 08326006
Hyphenated Format 0832-6006

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0308326006110 0308326004116
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 ANDA213784 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0832-6006-11)
source: ndc

Packages (1)

0832-6006-11 100 TABLET, FILM COATED in 1 BOTTLE (0832-6006-11)

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": "3bb74f82-8872-9829-e063-6294a90aeace", "openfda": {"upc": ["0308326006110", "0308326004116"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["f07bb3f1-c68c-441b-9de4-99a219f2500a"], "manufacturer_name": ["Upsher-Smith Laboratories,LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0832-6006-11)", "package_ndc": "0832-6006-11", "marketing_end_date": "20270731", "marketing_start_date": "20230302"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "0832-6006_3bb74f82-8872-9829-e063-6294a90aeace", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0832-6006", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Upsher-Smith Laboratories,LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213784", "marketing_category": "ANDA", "marketing_end_date": "20270731", "marketing_start_date": "20221122"}