Package 68788-4034-3

Brand: telmisartan

Generic: telmisartan
NDC Package

Package Facts

Identity

Package NDC 68788-4034-3
Digits Only 6878840343
Product NDC 68788-4034
Description

30 TABLET in 1 BOTTLE (68788-4034-3)

Marketing

Marketing Status
Marketed Since 2025-09-29
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": "bf8e95fa-d181-4b46-8609-497e14a73dc1", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["205304"], "spl_set_id": ["bf8e95fa-d181-4b46-8609-497e14a73dc1"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-4034-3)", "package_ndc": "68788-4034-3", "marketing_start_date": "20250929"}], "brand_name": "Telmisartan", "product_id": "68788-4034_bf8e95fa-d181-4b46-8609-497e14a73dc1", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68788-4034", "generic_name": "Telmisartan", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "40 mg/1"}], "application_number": "ANDA090032", "marketing_category": "ANDA", "marketing_start_date": "20250929", "listing_expiration_date": "20261231"}