Package 70518-3484-0

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3484-0
Digits Only 7051834840
Product NDC 70518-3484
Description

30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-3484-0)

Marketing

Marketing Status
Marketed Since 2022-08-19
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": "3a9d96fa-b59d-46cf-e063-6294a90a32df", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830861"], "spl_set_id": ["5e935265-d0fc-4223-835f-72426eeea6c4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-3484-0)", "package_ndc": "70518-3484-0", "marketing_start_date": "20220819"}], "brand_name": "diltiazem hydrochloride", "product_id": "70518-3484_3a9d96fa-b59d-46cf-e063-6294a90a32df", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "70518-3484", "generic_name": "diltiazem hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "diltiazem hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA208783", "marketing_category": "ANDA", "marketing_start_date": "20220819", "listing_expiration_date": "20261231"}