Package 71335-0579-2
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
71335-0579-2
Digits Only
7133505792
Product NDC
71335-0579
Description
90 TABLET in 1 BOTTLE (71335-0579-2)
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": "fd901e8d-53ca-6e15-e053-6294a90a4b31", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["831102"], "spl_set_id": ["225a87fb-d353-4ee7-bd08-14d631ff6b16"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0579-1)", "package_ndc": "71335-0579-1", "marketing_start_date": "20211227"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0579-2)", "package_ndc": "71335-0579-2", "marketing_start_date": "20180313"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "71335-0579_fd901e8d-53ca-6e15-e053-6294a90a4b31", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71335-0579", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "NDA018602", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}