Package 72189-344-90

Brand: cartia xt

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-344-90
Digits Only 7218934490
Product NDC 72189-344
Product ID 72189-344_2c4c7b35-cdc7-a9c1-e063-6394a90a7634
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-344-90)

Marketing

Marketing Status
Marketed Since 2022-04-06
Brand cartia xt
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

CARTIA XT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4c7b35-cdc7-a9c1-e063-6394a90a7634", "openfda": {"unii": ["OLH94387TE"], "spl_set_id": ["dbfda3a5-5602-6e47-e053-2995a90ac07b"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-344-90)", "package_ndc": "72189-344-90", "marketing_start_date": "20220406"}], "brand_name": "CARTIA XT", "product_id": "72189-344_2c4c7b35-cdc7-a9c1-e063-6394a90a7634", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "72189-344", "generic_name": "diltiazem hydrochloride", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARTIA XT", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA074752", "marketing_category": "ANDA", "marketing_start_date": "20220406", "listing_expiration_date": "20261231"}