Package 70518-2572-1

Brand: telmisartan

Generic: telmisartan
NDC Package

Package Facts

Identity

Package NDC 70518-2572-1
Digits Only 7051825721
Product NDC 70518-2572
Description

30 TABLET in 1 BOTTLE (70518-2572-1)

Marketing

Marketing Status
Marketed Since 2025-06-24
Brand telmisartan
Generic telmisartan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a6824b0-52cc-66ef-e063-6394a90a503f", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["205305"], "spl_set_id": ["91215664-6e19-4e04-9ae7-ab5664799426"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70518-2572-1)", "package_ndc": "70518-2572-1", "marketing_start_date": "20250624"}], "brand_name": "Telmisartan", "product_id": "70518-2572_4a6824b0-52cc-66ef-e063-6394a90a503f", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-2572", "generic_name": "Telmisartan", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "80 mg/1"}], "application_number": "ANDA090032", "marketing_category": "ANDA", "marketing_start_date": "20200210", "listing_expiration_date": "20271231"}