thioridazine hydrochloride

Generic: thioridazine hydrochloride

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

Drug Facts

Product Profile

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

thioridazine hydrochloride 50 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-938
Product ID 62135-938_2e81bd7d-c434-2d02-e063-6294a90a196d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088134
Listing Expiration 2026-12-31
Marketing Start 1983-08-30

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135938
Hyphenated Format 62135-938

Supplemental Identifiers

RxCUI
198270 198274 198275 313354
UPC
0362135934903 0362135936907 0362135939908 0362135938901
UNII
4WCI67NK8M

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 thioridazine hydrochloride (source: ndc)
Generic Name thioridazine hydrochloride (source: ndc)
Application Number ANDA088134 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (62135-938-90)
source: ndc

Packages (1)

62135-938-90 90 TABLET, FILM COATED in 1 BOTTLE (62135-938-90)

Ingredients (1)

thioridazine hydrochloride (50 mg/1)

Linked Drug Pages (1)

Thioridazine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2e81bd7d-c434-2d02-e063-6294a90a196d", "openfda": {"upc": ["0362135934903", "0362135936907", "0362135939908", "0362135938901"], "unii": ["4WCI67NK8M"], "rxcui": ["198270", "198274", "198275", "313354"], "spl_set_id": ["e0bbe982-6434-468b-bd29-64ac57386fbe"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-938-90)", "package_ndc": "62135-938-90", "marketing_start_date": "20250214"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "62135-938_2e81bd7d-c434-2d02-e063-6294a90a196d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62135-938", "generic_name": "Thioridazine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thioridazine Hydrochloride", "active_ingredients": [{"name": "THIORIDAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA088134", "marketing_category": "ANDA", "marketing_start_date": "19830830", "listing_expiration_date": "20261231"}