Package 82868-036-10

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-036-10
Digits Only 8286803610
Product NDC 82868-036
Product ID 82868-036_47f89c58-08d5-61d7-e063-6394a90a39a2
Description

10 TABLET in 1 BOTTLE, PLASTIC (82868-036-10)

Marketing

Marketing Status
Marketed Since 2024-01-18
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": "47f89c58-08d5-61d7-e063-6394a90a39a2", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["833217"], "spl_set_id": ["106b33e3-b199-e555-e063-6294a90a5af5"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (82868-036-10)", "package_ndc": "82868-036-10", "marketing_start_date": "20240118"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "82868-036_47f89c58-08d5-61d7-e063-6394a90a39a2", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "82868-036", "generic_name": "Diltiazem hydrochloride", "labeler_name": "Northwind Health Company, 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": "20240118", "listing_expiration_date": "20271231"}