Package 0615-8381-39
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
0615-8381-39
Digits Only
0615838139
Product NDC
0615-8381
Description
30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8381-39)
Marketing
Marketing Status
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": "72f92a1f-d8d6-494e-a8e9-875ca4bf4b50", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830837", "830845", "830861"], "spl_set_id": ["70f167a1-ec7f-4969-b446-166af3e52c05"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8381-39)", "package_ndc": "0615-8381-39", "marketing_start_date": "20210209"}], "brand_name": "diltiazem hydrochloride", "product_id": "0615-8381_72f92a1f-d8d6-494e-a8e9-875ca4bf4b50", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0615-8381", "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": "240 mg/1"}], "application_number": "ANDA208783", "marketing_category": "ANDA", "marketing_start_date": "20190614", "listing_expiration_date": "20261231"}