Package 68071-4242-3
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
68071-4242-3
Digits Only
6807142423
Product NDC
68071-4242
Description
30 TABLET in 1 BOTTLE (68071-4242-3)
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": "1a3c5c49-b375-1318-e063-6394a90a47b6", "openfda": {"upc": ["0368071424232"], "unii": ["OLH94387TE"], "rxcui": ["831054"], "spl_set_id": ["636556f6-2987-984f-e053-2991aa0a201a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4242-3)", "package_ndc": "68071-4242-3", "marketing_start_date": "20180122"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "68071-4242_1a3c5c49-b375-1318-e063-6394a90a47b6", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "68071-4242", "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": "NDA018602", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}