Package 71085-081-30

Brand: clemsza

Generic: clemastine fumarate
NDC Package

Package Facts

Identity

Package NDC 71085-081-30
Digits Only 7108508130
Product NDC 71085-081
Description

30 TABLET in 1 BOTTLE (71085-081-30)

Marketing

Marketing Status
Marketed Since 2025-08-01
Brand clemsza
Generic clemastine fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b2a232e-e840-b8e1-e063-6394a90ae51d", "openfda": {"unii": ["19259EGQ3D"], "rxcui": ["857461", "2720338"], "spl_set_id": ["9a35ed77-e35c-4c54-ad7f-1b92e450fa20"], "manufacturer_name": ["IPG Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71085-081-30)", "package_ndc": "71085-081-30", "marketing_start_date": "20250801"}], "brand_name": "CLEMSZA", "product_id": "71085-081_3b2a232e-e840-b8e1-e063-6394a90ae51d", "dosage_form": "TABLET", "product_ndc": "71085-081", "generic_name": "Clemastine Fumarate", "labeler_name": "IPG Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLEMSZA", "active_ingredients": [{"name": "CLEMASTINE FUMARATE", "strength": "2.68 mg/1"}], "application_number": "ANDA073283", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}