tiopronin

Generic: tiopronin

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

Drug Facts

Product Profile

Brand Name tiopronin
Generic Name tiopronin
Labeler teva pharmaceuticals, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

tiopronin 300 mg/1

Manufacturer
Teva Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0480-7824
Product ID 0480-7824_53891a64-8014-4b0b-9f13-cfc3d90166b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216456
Listing Expiration 2026-12-31
Marketing Start 2024-10-08

Pharmacologic Class

Established (EPC)
reducing and complexing thiol [epc]
Mechanism of Action
cystine disulfide reduction [moa]
Chemical Structure
n-substituted glycines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04807824
Hyphenated Format 0480-7824

Supplemental Identifiers

RxCUI
2178075 2178079
UNII
C5W04GO61S
NUI
N0000175549 M0289359 N0000175898

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 tiopronin (source: ndc)
Generic Name tiopronin (source: ndc)
Application Number ANDA216456 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0480-7824-98)
source: ndc

Packages (1)

Ingredients (1)

tiopronin (300 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "53891a64-8014-4b0b-9f13-cfc3d90166b2", "openfda": {"nui": ["N0000175549", "M0289359", "N0000175898"], "unii": ["C5W04GO61S"], "rxcui": ["2178075", "2178079"], "spl_set_id": ["749257d9-a519-4b10-9058-7fe3f301cdd2"], "pharm_class_cs": ["N-substituted Glycines [CS]"], "pharm_class_epc": ["Reducing and Complexing Thiol [EPC]"], "pharm_class_moa": ["Cystine Disulfide Reduction [MoA]"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (0480-7824-98)", "package_ndc": "0480-7824-98", "marketing_start_date": "20241008"}], "brand_name": "Tiopronin", "product_id": "0480-7824_53891a64-8014-4b0b-9f13-cfc3d90166b2", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cystine Disulfide Reduction [MoA]", "N-substituted Glycines [CS]", "Reducing and Complexing Thiol [EPC]"], "product_ndc": "0480-7824", "generic_name": "Tiopronin", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tiopronin", "active_ingredients": [{"name": "TIOPRONIN", "strength": "300 mg/1"}], "application_number": "ANDA216456", "marketing_category": "ANDA", "marketing_start_date": "20241008", "listing_expiration_date": "20261231"}