Package 0228-2918-09

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0228-2918-09
Digits Only 0228291809
Product NDC 0228-2918
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2918-09)

Marketing

Marketing Status
Marketed Since 2013-11-25
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": "3bfa9909-89ed-47d3-8e01-0c688a59a093", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830795"], "spl_set_id": ["178eec1f-1d4d-4a38-b66a-d3ba3de06c3d"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2918-09)", "package_ndc": "0228-2918-09", "marketing_start_date": "20131125"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "0228-2918_3bfa9909-89ed-47d3-8e01-0c688a59a093", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0228-2918", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "360 mg/1"}], "application_number": "ANDA202463", "marketing_category": "ANDA", "marketing_start_date": "20131125", "listing_expiration_date": "20261231"}