Package 63629-2127-1

Brand: candesartan cilexetil

Generic: candesartan cilexetil
NDC Package

Package Facts

Identity

Package NDC 63629-2127-1
Digits Only 6362921271
Product NDC 63629-2127
Product ID 63629-2127_a27d5502-a14f-4832-b342-c0d72d1c1257
Description

90 TABLET in 1 BOTTLE (63629-2127-1)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand candesartan cilexetil
Generic candesartan cilexetil
Sample Package No

Linked Drug Pages (1)

Candesartan cilexetil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a27d5502-a14f-4832-b342-c0d72d1c1257", "openfda": {"unii": ["R85M2X0D68"], "rxcui": ["153823"], "spl_set_id": ["2cdfc8ef-8418-4a2f-8cf3-769596fa9ac6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-2127-1)", "package_ndc": "63629-2127-1", "marketing_end_date": "20260430", "marketing_start_date": "20220831"}], "brand_name": "Candesartan cilexetil", "product_id": "63629-2127_a27d5502-a14f-4832-b342-c0d72d1c1257", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "63629-2127", "generic_name": "Candesartan cilexetil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Candesartan cilexetil", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "8 mg/1"}], "application_number": "NDA020838", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260430", "marketing_start_date": "20130521"}