Package 70748-195-07

Brand: sacubitril and valsartan

Generic: sacubitril and valsartan
NDC Package

Package Facts

Identity

Package NDC 70748-195-07
Digits Only 7074819507
Product NDC 70748-195
Description

60 TABLET, FILM COATED in 1 BOTTLE (70748-195-07)

Marketing

Marketing Status
Marketed Since 2025-07-29
Brand sacubitril and valsartan
Generic sacubitril and valsartan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e8c2bfce-cd97-4f79-a4e7-0c9ed648d7fa", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0370748196076", "0370748195079", "0370748197073"], "unii": ["80M03YXJ7I", "17ERJ0MKGI"], "rxcui": ["1656340", "1656349", "1656354"], "spl_set_id": ["76cbb87b-6356-4ead-af7f-faffb6e79743"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (70748-195-07)", "package_ndc": "70748-195-07", "marketing_start_date": "20250729"}], "brand_name": "sacubitril and valsartan", "product_id": "70748-195_e8c2bfce-cd97-4f79-a4e7-0c9ed648d7fa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Neprilysin Inhibitor [EPC]", "Neprilysin Inhibitors [MoA]"], "product_ndc": "70748-195", "generic_name": "sacubitril and valsartan", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sacubitril and valsartan", "active_ingredients": [{"name": "SACUBITRIL", "strength": "24 mg/1"}, {"name": "VALSARTAN", "strength": "26 mg/1"}], "application_number": "ANDA213808", "marketing_category": "ANDA", "marketing_start_date": "20250729", "listing_expiration_date": "20261231"}