Package 71335-3032-1

Brand: candesartan

Generic: candesartan
NDC Package

Package Facts

Identity

Package NDC 71335-3032-1
Digits Only 7133530321
Product NDC 71335-3032
Description

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

Marketing

Marketing Status
Marketed Since 2026-02-05
Brand candesartan
Generic candesartan
Sample Package No

Linked Drug Pages (1)

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"}