Package 63629-2154-1

Brand: diltiazem hydrochloride extended-release

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2154-1
Digits Only 6362921541
Product NDC 63629-2154
Description

30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2154-1)

Marketing

Marketing Status
Marketed Since 2021-03-10
Brand diltiazem hydrochloride extended-release
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "321ec15d-757f-491f-a5b9-742e68c5c6d5", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830861"], "spl_set_id": ["0e9b4421-bc43-4a77-b49b-e3f53d1e0f01"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2154-1)", "package_ndc": "63629-2154-1", "marketing_start_date": "20210310"}], "brand_name": "Diltiazem Hydrochloride Extended-Release", "product_id": "63629-2154_321ec15d-757f-491f-a5b9-742e68c5c6d5", "dosage_form": "CAPSULE, COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "63629-2154", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA074984", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}