Package 68382-598-77
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
68382-598-77
Digits Only
6838259877
Product NDC
68382-598
Description
10 BLISTER PACK in 1 CARTON (68382-598-77) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68382-598-30)
Marketing
Marketing Status
Brand
diltiazem hydrochloride
Generic
diltiazem hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3683dc39-602e-463a-b04a-6d066d2fe94d", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830795", "830801", "830837", "830845", "830861"], "spl_set_id": ["1e2f2025-0350-40c4-ab42-3b57f3d105a6"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-598-01)", "package_ndc": "68382-598-01", "marketing_start_date": "20170928"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-598-05)", "package_ndc": "68382-598-05", "marketing_start_date": "20181002"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-598-06)", "package_ndc": "68382-598-06", "marketing_start_date": "20170928"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-598-16)", "package_ndc": "68382-598-16", "marketing_start_date": "20170928"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-598-77) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68382-598-30)", "package_ndc": "68382-598-77", "marketing_start_date": "20170928"}], "brand_name": "diltiazem hydrochloride", "product_id": "68382-598_3683dc39-602e-463a-b04a-6d066d2fe94d", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "68382-598", "generic_name": "diltiazem hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "diltiazem hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA206534", "marketing_category": "ANDA", "marketing_start_date": "20170928", "listing_expiration_date": "20261231"}