Package 67046-1481-3

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1481-3
Digits Only 6704614813
Product NDC 67046-1481
Description

30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1481-3)

Marketing

Marketing Status
Marketed Since 2025-01-30
Brand diltiazem hydrochloride
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ced5dc5-47e0-1b71-e063-6394a90a0e3d", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830872"], "spl_set_id": ["2ced821f-19a6-4c7e-e063-6394a90adb80"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1481-3)", "package_ndc": "67046-1481-3", "marketing_start_date": "20250130"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "67046-1481_2ced5dc5-47e0-1b71-e063-6394a90a0e3d", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "67046-1481", "generic_name": "diltiazem hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA074910", "marketing_category": "ANDA", "marketing_start_date": "20250130", "listing_expiration_date": "20261231"}