Package 68682-105-10

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 68682-105-10
Digits Only 6868210510
Product NDC 68682-105
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-10)

Marketing

Marketing Status
Marketed Since 2012-10-18
Brand nifedipine
Generic nifedipine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ed2ab44d-7e6a-4c65-8bb0-9d3a4d9bf618", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198034"], "spl_set_id": ["cb051508-60f3-4b89-9da0-5261024bd7f4"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-10)", "package_ndc": "68682-105-10", "marketing_start_date": "20121018"}, {"sample": false, "description": "300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-30)", "package_ndc": "68682-105-30", "marketing_start_date": "20121018"}], "brand_name": "Nifedipine", "product_id": "68682-105_ed2ab44d-7e6a-4c65-8bb0-9d3a4d9bf618", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68682-105", "generic_name": "Nifedipine", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA075269", "marketing_category": "ANDA", "marketing_start_date": "20121018", "listing_expiration_date": "20271231"}