Package 65862-740-03
Brand: amlodipine and valsartan
Generic: amlodipine and valsartanPackage Facts
Identity
Package NDC
65862-740-03
Digits Only
6586274003
Product NDC
65862-740
Description
3 BLISTER PACK in 1 CARTON (65862-740-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-740-10)
Marketing
Marketing Status
Brand
amlodipine and valsartan
Generic
amlodipine and valsartan
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "909d72a6-7116-407e-8ec8-77b9b5798237", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0365862739308", "0365862737304"], "unii": ["864V2Q084H", "80M03YXJ7I"], "rxcui": ["722126", "722131", "722134", "722137"], "spl_set_id": ["7fa25f10-29e0-4162-81a8-9d2e03054ded"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (65862-740-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-740-10)", "package_ndc": "65862-740-03", "marketing_start_date": "20160422"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-740-30)", "package_ndc": "65862-740-30", "marketing_start_date": "20160422"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-740-90)", "package_ndc": "65862-740-90", "marketing_start_date": "20160422"}], "brand_name": "Amlodipine and valsartan", "product_id": "65862-740_909d72a6-7116-407e-8ec8-77b9b5798237", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "65862-740", "generic_name": "Amlodipine and valsartan", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and valsartan", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA206512", "marketing_category": "ANDA", "marketing_start_date": "20160422", "listing_expiration_date": "20261231"}