Package 68682-707-90

{"route": ["ORAL"], "spl_id": "9c3468f2-1199-4180-9e57-089b5353251a", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830874", "830877", "830879", "830882", "830897", "830900"], "spl_set_id": ["73b3607a-99d0-44d8-92ef-0074684c9d7d"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-707-30)", "package_ndc": "68682-707-30", "marketing_start_date": "20140206"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-707-90)", "package_ndc": "68682-707-90", "marketing_start_date": "20140206"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "68682-707_9c3468f2-1199-4180-9e57-089b5353251a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "68682-707", "generic_name": "Diltiazem Hydrochloride Extended-Release Tablets", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "NDA021392", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20140206", "listing_expiration_date": "20261231"}