trifluoperazine hydrochloride
Generic: trifluoperazine hydrochloride
Labeler: mylan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
trifluoperazine hydrochloride
Generic Name
trifluoperazine hydrochloride
Labeler
mylan pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
trifluoperazine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0378-2405
Product ID
0378-2405_7586125c-d9c7-4c56-8ca8-8add657a91db
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040209
Listing Expiration
2026-12-31
Marketing Start
1997-08-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03782405
Hyphenated Format
0378-2405
Supplemental Identifiers
RxCUI
UPC
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
trifluoperazine hydrochloride (source: ndc)
Generic Name
trifluoperazine hydrochloride (source: ndc)
Application Number
ANDA040209 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2405-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7586125c-d9c7-4c56-8ca8-8add657a91db", "openfda": {"upc": ["0303782402018", "0303782405019"], "unii": ["6P1Y2SNF5V"], "rxcui": ["198322", "198323", "198324", "198325"], "spl_set_id": ["c2575a86-19e5-44df-8603-ff066bb9c9c5"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2405-01)", "package_ndc": "0378-2405-01", "marketing_start_date": "19970829"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "0378-2405_7586125c-d9c7-4c56-8ca8-8add657a91db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0378-2405", "generic_name": "trifluoperazine hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA040209", "marketing_category": "ANDA", "marketing_start_date": "19970829", "listing_expiration_date": "20261231"}