thioridazine hydrochloride

Generic: thioridazine hydrochloride

Labeler: mylan institutional inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name thioridazine hydrochloride
Generic Name thioridazine hydrochloride
Labeler mylan institutional inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

thioridazine hydrochloride 100 mg/1

Manufacturer
Mylan Institutional Inc.

Identifiers & Regulatory

Product NDC 51079-580
Product ID 51079-580_4358c933-3022-792d-e063-6294a90aacb6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088004
Listing Expiration 2026-12-31
Marketing Start 1998-06-22

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51079580
Hyphenated Format 51079-580

Supplemental Identifiers

RxCUI
198270 198274 198275 313354
UNII
4WCI67NK8M

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 ANDA088004 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (51079-580-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-580-01)
source: ndc

Packages (1)

Ingredients (1)

thioridazine hydrochloride (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4358c933-3022-792d-e063-6294a90aacb6", "openfda": {"unii": ["4WCI67NK8M"], "rxcui": ["198270", "198274", "198275", "313354"], "spl_set_id": ["52fea941-0b47-41c1-b00d-f88150e8ab93"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-580-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-580-01)", "package_ndc": "51079-580-20", "marketing_start_date": "19980622"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "51079-580_4358c933-3022-792d-e063-6294a90aacb6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51079-580", "generic_name": "thioridazine hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thioridazine Hydrochloride", "active_ingredients": [{"name": "THIORIDAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA088004", "marketing_category": "ANDA", "marketing_start_date": "19980622", "listing_expiration_date": "20261231"}