candesartan cilexetil

Generic: candesartan cilexetil

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name candesartan cilexetil
Generic Name candesartan cilexetil
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

candesartan cilexetil 4 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-341
Product ID 62332-341_5a3c0018-b0e2-4fe7-bec7-c075f50833ec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210302
Listing Expiration 2026-12-31
Marketing Start 2018-12-05

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 62332341
Hyphenated Format 62332-341

Supplemental Identifiers

RxCUI
153822 153823 577776
UPC
0362332341306 0362332342303
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 ANDA210302 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (62332-341-30)
  • 90 TABLET in 1 BOTTLE (62332-341-90)
  • 1000 TABLET in 1 BOTTLE (62332-341-91)
source: ndc

Packages (3)

62332-341-30 30 TABLET in 1 BOTTLE (62332-341-30) 62332-341-90 90 TABLET in 1 BOTTLE (62332-341-90) 62332-341-91 1000 TABLET in 1 BOTTLE (62332-341-91)

Ingredients (1)

candesartan cilexetil (4 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": "5a3c0018-b0e2-4fe7-bec7-c075f50833ec", "openfda": {"upc": ["0362332341306", "0362332342303"], "unii": ["R85M2X0D68"], "rxcui": ["153822", "153823", "577776"], "spl_set_id": ["8a515af5-bd53-43f1-b40a-aa0f332bc2ab"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-341-30)", "package_ndc": "62332-341-30", "marketing_start_date": "20181205"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62332-341-90)", "package_ndc": "62332-341-90", "marketing_start_date": "20181205"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-341-91)", "package_ndc": "62332-341-91", "marketing_start_date": "20181205"}], "brand_name": "CANDESARTAN CILEXETIL", "product_id": "62332-341_5a3c0018-b0e2-4fe7-bec7-c075f50833ec", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62332-341", "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": "4 mg/1"}], "application_number": "ANDA210302", "marketing_category": "ANDA", "marketing_start_date": "20181205", "listing_expiration_date": "20261231"}