Package 0187-2049-90

Brand: cardizem la

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0187-2049-90
Digits Only 0187204990
Product NDC 0187-2049
Product ID 0187-2049_1771fff3-92c3-48ee-b786-5d6d7c6e6628
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-90)

Marketing

Marketing Status
Marketed Since 2010-12-25
Brand cardizem la
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Cardizem LA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1771fff3-92c3-48ee-b786-5d6d7c6e6628", "openfda": {"upc": ["0301872045909", "0301872047903"], "unii": ["OLH94387TE"], "rxcui": ["830874", "830876", "830877", "830878", "830879", "830880", "830882", "830883", "830897", "830898", "830900", "830902"], "spl_set_id": ["3e180dc7-c871-4efc-8755-cae882976c8d"], "manufacturer_name": ["Bausch Health US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-30)", "package_ndc": "0187-2049-30", "marketing_start_date": "20101225"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-90)", "package_ndc": "0187-2049-90", "marketing_start_date": "20101225"}], "brand_name": "Cardizem LA", "product_id": "0187-2049_1771fff3-92c3-48ee-b786-5d6d7c6e6628", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0187-2049", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bausch Health US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cardizem LA", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "360 mg/1"}], "application_number": "NDA021392", "marketing_category": "NDA", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}