Package 70518-3556-0

Brand: telmisartan

Generic: telmisartan
NDC Package

Package Facts

Identity

Package NDC 70518-3556-0
Digits Only 7051835560
Product NDC 70518-3556
Description

30 TABLET in 1 BOTTLE (70518-3556-0)

Marketing

Marketing Status
Marketed Since 2022-10-17
Brand telmisartan
Generic telmisartan
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f1670a2-6b4e-6b11-e063-6294a90a661c", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["205305"], "spl_set_id": ["57da6ef2-2e86-4e4d-90df-73a2a8cf97f6"], "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 (70518-3556-0)", "package_ndc": "70518-3556-0", "marketing_start_date": "20221017"}], "brand_name": "Telmisartan", "product_id": "70518-3556_3f1670a2-6b4e-6b11-e063-6294a90a661c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-3556", "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": "ANDA207882", "marketing_category": "ANDA", "marketing_start_date": "20221017", "listing_expiration_date": "20261231"}