Package 49884-659-09

Brand: candesartan cilexetil

Generic: candesartan cilexetil
NDC Package

Package Facts

Identity

Package NDC 49884-659-09
Digits Only 4988465909
Product NDC 49884-659
Product ID 49884-659_fc8868a3-89f5-4414-b3c8-edece3b529f4
Description

90 TABLET in 1 BOTTLE (49884-659-09)

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": "fc8868a3-89f5-4414-b3c8-edece3b529f4", "openfda": {"unii": ["R85M2X0D68"], "rxcui": ["153822", "153823", "577776", "639537"], "spl_set_id": ["1c90aa68-cc12-41ef-aebc-2616ae45683a"], "manufacturer_name": ["Par Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (49884-659-09)", "package_ndc": "49884-659-09", "marketing_end_date": "20260430", "marketing_start_date": "20130521"}], "brand_name": "Candesartan cilexetil", "product_id": "49884-659_fc8868a3-89f5-4414-b3c8-edece3b529f4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "49884-659", "generic_name": "Candesartan cilexetil", "labeler_name": "Par Pharmaceutical Inc.", "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"}