Package 0603-3582-21
Brand: felodipine
Generic: felodipinePackage Facts
Identity
Package NDC
0603-3582-21
Digits Only
0603358221
Product NDC
0603-3582
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3582-21)
Marketing
Marketing Status
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": "ca215c73-f6f1-492c-810c-876e46001086", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["OL961R6O2C"], "rxcui": ["402695", "402696", "402698"], "spl_set_id": ["55637724-8757-11de-8a39-0800200c9a66"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3582-21)", "package_ndc": "0603-3582-21", "marketing_start_date": "20111215"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3582-28)", "package_ndc": "0603-3582-28", "marketing_start_date": "20111215"}], "brand_name": "Felodipine", "product_id": "0603-3582_ca215c73-f6f1-492c-810c-876e46001086", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "0603-3582", "generic_name": "Felodipine", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felodipine", "active_ingredients": [{"name": "FELODIPINE", "strength": "5 mg/1"}], "application_number": "ANDA200815", "marketing_category": "ANDA", "marketing_start_date": "20111215", "listing_expiration_date": "20261231"}