Package 10370-832-05
Brand: diltiazem hydrochloride extended-release
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
10370-832-05
Digits Only
1037083205
Product NDC
10370-832
Description
500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (10370-832-05)
Marketing
Marketing Status
Brand
diltiazem hydrochloride extended-release
Generic
diltiazem hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c13ca26-597e-4886-b085-85bc95eb3ceb", "openfda": {"upc": ["0310370832058", "0310370830092", "0310370831099", "0310370831051", "0310370829096", "0310370832119", "0310370832096", "0310370831112", "0310370830115", "0310370830054"], "unii": ["OLH94387TE"], "rxcui": ["830801", "830837", "830845", "830861"], "spl_set_id": ["a66ad880-cdab-435a-a6f2-574cfdfd1ac3"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (10370-832-05)", "package_ndc": "10370-832-05", "marketing_start_date": "20170526"}, {"sample": false, "description": "90 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (10370-832-09)", "package_ndc": "10370-832-09", "marketing_start_date": "20170407"}, {"sample": false, "description": "30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (10370-832-11)", "package_ndc": "10370-832-11", "marketing_start_date": "20170522"}], "brand_name": "Diltiazem Hydrochloride Extended-Release", "product_id": "10370-832_0c13ca26-597e-4886-b085-85bc95eb3ceb", "dosage_form": "CAPSULE, COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "10370-832", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA074984", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}