venxxiva

Generic: tiopronin

Labeler: cycle pharmaceuticals ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venxxiva
Generic Name tiopronin
Labeler cycle pharmaceuticals ltd.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

tiopronin 300 mg/1

Manufacturer
Cycle Pharmaceuticals Ltd.

Identifiers & Regulatory

Product NDC 70709-123
Product ID 70709-123_c8eeb4d4-9718-41ba-b4fe-3d645fd60a20
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216990
Listing Expiration 2026-12-31
Marketing Start 2025-01-22

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 70709123
Hyphenated Format 70709-123

Supplemental Identifiers

RxCUI
2178075 2178079 2702682 2702684
UPC
0370709123905 0370709121307
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 venxxiva (source: ndc)
Generic Name tiopronin (source: ndc)
Application Number ANDA216990 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (70709-123-90)
source: ndc

Packages (1)

70709-123-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (70709-123-90)

Ingredients (1)

tiopronin (300 mg/1)

Linked Drug Pages (1)

VENXXIVA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c8eeb4d4-9718-41ba-b4fe-3d645fd60a20", "openfda": {"nui": ["N0000175549", "M0289359", "N0000175898"], "upc": ["0370709123905", "0370709121307"], "unii": ["C5W04GO61S"], "rxcui": ["2178075", "2178079", "2702682", "2702684"], "spl_set_id": ["02e24443-04c6-4b98-a395-49aec4a468de"], "pharm_class_cs": ["N-substituted Glycines [CS]"], "pharm_class_epc": ["Reducing and Complexing Thiol [EPC]"], "pharm_class_moa": ["Cystine Disulfide Reduction [MoA]"], "manufacturer_name": ["Cycle Pharmaceuticals Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (70709-123-90)", "package_ndc": "70709-123-90", "marketing_start_date": "20250122"}], "brand_name": "VENXXIVA", "product_id": "70709-123_c8eeb4d4-9718-41ba-b4fe-3d645fd60a20", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cystine Disulfide Reduction [MoA]", "N-substituted Glycines [CS]", "Reducing and Complexing Thiol [EPC]"], "product_ndc": "70709-123", "generic_name": "tiopronin", "labeler_name": "Cycle Pharmaceuticals Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENXXIVA", "active_ingredients": [{"name": "TIOPRONIN", "strength": "300 mg/1"}], "application_number": "ANDA216990", "marketing_category": "ANDA", "marketing_start_date": "20250122", "listing_expiration_date": "20261231"}