Package 80705-120-30

Brand: carbinoxamine maleate

Generic: carbinoxamine maleate
NDC Package

Package Facts

Identity

Package NDC 80705-120-30
Digits Only 8070512030
Product NDC 80705-120
Description

30 TABLET in 1 BOTTLE (80705-120-30)

Marketing

Marketing Status
Marketed Since 2025-07-22
Brand carbinoxamine maleate
Generic carbinoxamine maleate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "28237aea-8a3c-40ca-b2a1-0b7248ce5b99", "openfda": {"upc": ["0380705120303"], "unii": ["02O55696WH"], "rxcui": ["1795581"], "spl_set_id": ["91ee2e99-082a-4157-b71b-1a7c0e5464fa"], "manufacturer_name": ["TRIPOINT THERAPEUTICS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80705-120-30)", "package_ndc": "80705-120-30", "marketing_start_date": "20250722"}], "brand_name": "Carbinoxamine Maleate", "product_id": "80705-120_28237aea-8a3c-40ca-b2a1-0b7248ce5b99", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "80705-120", "generic_name": "Carbinoxamine Maleate", "labeler_name": "TRIPOINT THERAPEUTICS, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbinoxamine Maleate", "active_ingredients": [{"name": "CARBINOXAMINE MALEATE", "strength": "6 mg/1"}], "application_number": "ANDA215476", "marketing_category": "ANDA", "marketing_start_date": "20250722", "listing_expiration_date": "20261231"}