Package 68462-234-10

Brand: felodipine

Generic: felodipine
NDC Package

Package Facts

Identity

Package NDC 68462-234-10
Digits Only 6846223410
Product NDC 68462-234
Description

1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-234-10)

Marketing

Marketing Status
Marketed Since 2010-12-20
Brand felodipine
Generic felodipine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8663994d-841f-427a-93db-b4c9d10bad27", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0368462235010", "0368462233016", "0368462234013"], "unii": ["OL961R6O2C"], "rxcui": ["402695", "402696", "402698"], "spl_set_id": ["2e4298cf-02e9-49c7-9803-887161e1989a"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-234-01)", "package_ndc": "68462-234-01", "marketing_start_date": "20101220"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-234-10)", "package_ndc": "68462-234-10", "marketing_start_date": "20101220"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68462-234-11)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "68462-234-11", "marketing_start_date": "20101220"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-234-90)", "package_ndc": "68462-234-90", "marketing_start_date": "20101220"}], "brand_name": "Felodipine", "product_id": "68462-234_8663994d-841f-427a-93db-b4c9d10bad27", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68462-234", "generic_name": "Felodipine", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felodipine", "active_ingredients": [{"name": "FELODIPINE", "strength": "5 mg/1"}], "application_number": "ANDA090365", "marketing_category": "ANDA", "marketing_start_date": "20101220", "listing_expiration_date": "20271231"}