Package 68682-106-30

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 68682-106-30
Digits Only 6868210630
Product NDC 68682-106
Description

300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-106-30)

Marketing

Marketing Status
Marketed Since 2000-12-04
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": "2c9ac184-8e21-479c-a1e8-4abeadfb54a1", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198035"], "spl_set_id": ["fb6d8f32-198e-4ccf-bf25-069c03d624fd"], "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 (68682-106-10)", "package_ndc": "68682-106-10", "marketing_start_date": "20001204"}, {"sample": false, "description": "300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-106-30)", "package_ndc": "68682-106-30", "marketing_start_date": "20001204"}], "brand_name": "Nifedipine", "product_id": "68682-106_2c9ac184-8e21-479c-a1e8-4abeadfb54a1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68682-106", "generic_name": "Nifedipine", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "60 mg/1"}], "application_number": "ANDA075269", "marketing_category": "ANDA", "marketing_start_date": "20001204", "listing_expiration_date": "20271231"}