Package 68071-4664-3

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4664-3
Digits Only 6807146643
Product NDC 68071-4664
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4664-3)

Marketing

Marketing Status
Marketed Since 2018-12-12
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": "1ab86011-6c6d-e459-e063-6394a90a20dd", "openfda": {"upc": ["0368071466430"], "unii": ["OLH94387TE"], "rxcui": ["830861"], "spl_set_id": ["7cdb473a-e6d5-48e8-e053-2a91aa0aaeb7"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4664-3)", "package_ndc": "68071-4664-3", "marketing_start_date": "20181212"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "68071-4664_1ab86011-6c6d-e459-e063-6394a90a20dd", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "68071-4664", "generic_name": "Diltiazem hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA075116", "marketing_category": "ANDA", "marketing_start_date": "19991228", "listing_expiration_date": "20261231"}