thioridazine hydrochloride

Generic: thioridazine hydrochloride

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

Drug Facts

Product Profile

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

thioridazine hydrochloride 10 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0378-0612
Product ID 0378-0612_6437f615-1e2b-4d0a-ba83-a0c14391693d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088004
Listing Expiration 2026-12-31
Marketing Start 1983-03-15

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03780612
Hyphenated Format 0378-0612

Supplemental Identifiers

RxCUI
198270 198274 198275 313354
UPC
0303780618015 0303780616011 0303780612013 0303780614017
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 ANDA088004 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0612-01)
source: ndc

Packages (1)

0378-0612-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0612-01)

Ingredients (1)

thioridazine hydrochloride (10 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": "6437f615-1e2b-4d0a-ba83-a0c14391693d", "openfda": {"upc": ["0303780618015", "0303780616011", "0303780612013", "0303780614017"], "unii": ["4WCI67NK8M"], "rxcui": ["198270", "198274", "198275", "313354"], "spl_set_id": ["56b3f4c2-52af-4947-b225-6808ae9f26f5"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0612-01)", "package_ndc": "0378-0612-01", "marketing_start_date": "19830315"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "0378-0612_6437f615-1e2b-4d0a-ba83-a0c14391693d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0378-0612", "generic_name": "thioridazine hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thioridazine Hydrochloride", "active_ingredients": [{"name": "THIORIDAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088004", "marketing_category": "ANDA", "marketing_start_date": "19830315", "listing_expiration_date": "20261231"}