candesartan cilexetil
Generic: candesartan cilexetil
Labeler: alembic pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
candesartan cilexetil
Generic Name
candesartan cilexetil
Labeler
alembic pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
candesartan cilexetil 32 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62332-060
Product ID
62332-060_55b443a9-6652-4408-a91d-7aa4dbc457f9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209119
Listing Expiration
2026-12-31
Marketing Start
2017-06-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62332060
Hyphenated Format
62332-060
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA209119 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 32 mg/1
Packaging
- 100 TABLET in 1 CARTON (62332-060-10)
- 30 TABLET in 1 BOTTLE (62332-060-30)
- 90 TABLET in 1 BOTTLE (62332-060-90)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "55b443a9-6652-4408-a91d-7aa4dbc457f9", "openfda": {"upc": ["0362332060306"], "unii": ["R85M2X0D68"], "rxcui": ["639537"], "spl_set_id": ["0f2b2fa3-249b-4756-a3f1-3223a004d9cb"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (62332-060-10)", "package_ndc": "62332-060-10", "marketing_start_date": "20170621"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-060-30)", "package_ndc": "62332-060-30", "marketing_start_date": "20170621"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62332-060-90)", "package_ndc": "62332-060-90", "marketing_start_date": "20170621"}], "brand_name": "CANDESARTAN CILEXETIL", "product_id": "62332-060_55b443a9-6652-4408-a91d-7aa4dbc457f9", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62332-060", "generic_name": "CANDESARTAN CILEXETIL", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CANDESARTAN CILEXETIL", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "32 mg/1"}], "application_number": "ANDA209119", "marketing_category": "ANDA", "marketing_start_date": "20170621", "listing_expiration_date": "20261231"}