Package 84549-319-05

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-319-05
Digits Only 8454931905
Product NDC 84549-319
Product ID 84549-319_3f2942d7-f4d1-2d77-e063-6294a90a74ad
Description

5 mL in 1 VIAL (84549-319-05)

Marketing

Marketing Status
Marketed Since 2025-09-18
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": ["INTRAVENOUS"], "spl_id": "3f2942d7-f4d1-2d77-e063-6294a90a74ad", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["1791229"], "spl_set_id": ["3f2942d7-f4d0-2d77-e063-6294a90a74ad"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL (84549-319-05)", "package_ndc": "84549-319-05", "marketing_start_date": "20250918"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "84549-319_3f2942d7-f4d1-2d77-e063-6294a90a74ad", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "84549-319", "generic_name": "diltiazem hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA074617", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}