candesartan cilexetil

Generic: candesartan cilexetil

Labeler: par pharmaceutical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name candesartan cilexetil
Generic Name candesartan cilexetil
Labeler par pharmaceutical inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

candesartan cilexetil 8 mg/1

Manufacturer
Par Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 49884-659
Product ID 49884-659_fc8868a3-89f5-4414-b3c8-edece3b529f4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020838
Marketing Start 2013-05-21
Marketing End 2026-04-30

Pharmacologic Class

Classes
angiotensin 2 receptor antagonists [moa] angiotensin 2 receptor blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49884659
Hyphenated Format 49884-659

Supplemental Identifiers

RxCUI
153822 153823 577776 639537
UNII
R85M2X0D68

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name candesartan cilexetil (source: ndc)
Generic Name candesartan cilexetil (source: ndc)
Application Number NDA020838 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (49884-659-09)
source: ndc

Packages (1)

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

Ingredients (1)

candesartan cilexetil (8 mg/1)

Linked Drug Pages (1)

Candesartan cilexetil ndc-match (0.9)

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"}