Package 0615-8033-39

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8033-39
Digits Only 0615803339
Product NDC 0615-8033
Product ID 0615-8033_f396d205-71ac-4e1a-b989-a6a2c2da9677
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8033-39)

Marketing

Marketing Status
Marketed Since 2016-05-17
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": "f396d205-71ac-4e1a-b989-a6a2c2da9677", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["831103", "833217"], "spl_set_id": ["74620be9-5120-491a-a171-e50612c06541"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8033-39)", "package_ndc": "0615-8033-39", "marketing_start_date": "20160517"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "0615-8033_f396d205-71ac-4e1a-b989-a6a2c2da9677", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0615-8033", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA074185", "marketing_category": "ANDA", "marketing_start_date": "19951222", "listing_expiration_date": "20261231"}