candesartan

Generic: candesartan

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name candesartan
Generic Name candesartan
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

candesartan cilexetil 16 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-3032
Product ID 71335-3032_eeef5a15-6a83-4012-aee3-486668b243a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203813
Listing Expiration 2027-12-31
Marketing Start 2016-12-06

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 713353032
Hyphenated Format 71335-3032

Supplemental Identifiers

RxCUI
577776
UNII
R85M2X0D68

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 (source: ndc)
Generic Name candesartan (source: ndc)
Application Number ANDA203813 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 16 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-3032-1)
  • 90 TABLET in 1 BOTTLE (71335-3032-2)
source: ndc

Packages (2)

71335-3032-1 30 TABLET in 1 BOTTLE (71335-3032-1) 71335-3032-2 90 TABLET in 1 BOTTLE (71335-3032-2)

Ingredients (1)

candesartan cilexetil (16 mg/1)

Linked Drug Pages (1)

Candesartan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eeef5a15-6a83-4012-aee3-486668b243a2", "openfda": {"unii": ["R85M2X0D68"], "rxcui": ["577776"], "spl_set_id": ["7eb297cb-ef1b-44e0-a49d-03727100579e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-3032-1)", "package_ndc": "71335-3032-1", "marketing_start_date": "20260205"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-3032-2)", "package_ndc": "71335-3032-2", "marketing_start_date": "20260205"}], "brand_name": "Candesartan", "product_id": "71335-3032_eeef5a15-6a83-4012-aee3-486668b243a2", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-3032", "generic_name": "Candesartan", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Candesartan", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "16 mg/1"}], "application_number": "ANDA203813", "marketing_category": "ANDA", "marketing_start_date": "20161206", "listing_expiration_date": "20271231"}