Package 70771-1031-4

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70771-1031-4
Digits Only 7077110314
Product NDC 70771-1031
Description

10 BLISTER PACK in 1 CARTON (70771-1031-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-09-28
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": "99889af0-9650-495d-9834-3cb0e77cda5e", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830795", "830801", "830837", "830845", "830861"], "spl_set_id": ["fe790439-85d4-4cd8-a385-149ea3442a38"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1031-1)", "package_ndc": "70771-1031-1", "marketing_start_date": "20170928"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1031-3)", "package_ndc": "70771-1031-3", "marketing_start_date": "20170928"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1031-4)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "70771-1031-4", "marketing_start_date": "20170928"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1031-5)", "package_ndc": "70771-1031-5", "marketing_start_date": "20181002"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1031-9)", "package_ndc": "70771-1031-9", "marketing_start_date": "20170928"}], "brand_name": "diltiazem hydrochloride", "product_id": "70771-1031_99889af0-9650-495d-9834-3cb0e77cda5e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "70771-1031", "generic_name": "diltiazem hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "diltiazem hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA206534", "marketing_category": "ANDA", "marketing_start_date": "20170928", "listing_expiration_date": "20261231"}