Package 63629-3659-1

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-3659-1
Digits Only 6362936591
Product NDC 63629-3659
Product ID 63629-3659_c0d753f2-73e1-42a6-92c2-35718c3e53a6
Description

90 TABLET, FILM COATED in 1 BOTTLE (63629-3659-1)

Marketing

Marketing Status
Marketed Since 2024-03-27
Brand diltiazem hydrochloride
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Diltiazem Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c0d753f2-73e1-42a6-92c2-35718c3e53a6", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["833217"], "spl_set_id": ["6ca6a648-fc67-4cf8-a1f7-787c9574e3a1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-3659-1)", "package_ndc": "63629-3659-1", "marketing_start_date": "20240327"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "63629-3659_c0d753f2-73e1-42a6-92c2-35718c3e53a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "63629-3659", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA074185", "marketing_category": "ANDA", "marketing_start_date": "19951222", "listing_expiration_date": "20261231"}