Package 72603-721-01

Brand: candesartan

Generic: candesartan
NDC Package

Package Facts

Identity

Package NDC 72603-721-01
Digits Only 7260372101
Product NDC 72603-721
Product ID 72603-721_400810c5-9f59-4285-a3f6-fa98bba0c6a0
Description

90 TABLET in 1 CARTON (72603-721-01)

Marketing

Marketing Status
Marketed Since 2025-01-29
Brand candesartan
Generic candesartan
Sample Package No

Linked Drug Pages (1)

Candesartan ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "400810c5-9f59-4285-a3f6-fa98bba0c6a0", "openfda": {"unii": ["R85M2X0D68"], "rxcui": ["577776", "639537"], "spl_set_id": ["880f685f-be01-42f4-9e76-ebd1fcfb1f77"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 CARTON (72603-721-01)", "package_ndc": "72603-721-01", "marketing_start_date": "20250129"}], "brand_name": "Candesartan", "product_id": "72603-721_400810c5-9f59-4285-a3f6-fa98bba0c6a0", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72603-721", "generic_name": "Candesartan", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Candesartan", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "32 mg/1"}], "application_number": "ANDA203813", "marketing_category": "ANDA", "marketing_start_date": "20250129", "listing_expiration_date": "20261231"}