Package 67046-1492-3

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1492-3
Digits Only 6704614923
Product NDC 67046-1492
Product ID 67046-1492_2cd90eaf-cc66-7b68-e063-6294a90a9737
Description

30 TABLET in 1 BLISTER PACK (67046-1492-3)

Marketing

Marketing Status
Marketed Since 2025-01-29
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": "2cd90eaf-cc66-7b68-e063-6294a90a9737", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["833217"], "spl_set_id": ["2cd92b83-075e-b069-e063-6294a90a9fff"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1492-3)", "package_ndc": "67046-1492-3", "marketing_start_date": "20250129"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "67046-1492_2cd90eaf-cc66-7b68-e063-6294a90a9737", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "67046-1492", "generic_name": "Diltiazem hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA216521", "marketing_category": "ANDA", "marketing_start_date": "20250129", "listing_expiration_date": "20261231"}