candesartan

Generic: candesartan

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name candesartan
Generic Name candesartan
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

candesartan cilexetil 16 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-720
Product ID 72603-720_400810c5-9f59-4285-a3f6-fa98bba0c6a0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203813
Listing Expiration 2026-12-31
Marketing Start 2025-01-29

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 72603720
Hyphenated Format 72603-720

Supplemental Identifiers

RxCUI
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 (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
  • 90 TABLET in 1 CARTON (72603-720-01)
source: ndc

Packages (1)

72603-720-01 90 TABLET in 1 CARTON (72603-720-01)

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": "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 (72603-720-01)", "package_ndc": "72603-720-01", "marketing_start_date": "20250129"}], "brand_name": "Candesartan", "product_id": "72603-720_400810c5-9f59-4285-a3f6-fa98bba0c6a0", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72603-720", "generic_name": "Candesartan", "labeler_name": "NorthStar RxLLC", "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": "20250129", "listing_expiration_date": "20261231"}