Package 71335-2373-1

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2373-1
Digits Only 7133523731
Product NDC 71335-2373
Product ID 71335-2373_ce93c85d-fd72-4fb7-94ee-9338518e1f45
Description

90 TABLET in 1 BOTTLE (71335-2373-1)

Marketing

Marketing Status
Marketed Since 2024-05-23
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": "ce93c85d-fd72-4fb7-94ee-9338518e1f45", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["833217"], "spl_set_id": ["76e04232-b3da-48e8-a944-5f4f97a508df"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2373-1)", "package_ndc": "71335-2373-1", "marketing_start_date": "20240523"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "71335-2373_ce93c85d-fd72-4fb7-94ee-9338518e1f45", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71335-2373", "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": "30 mg/1"}], "application_number": "ANDA216521", "marketing_category": "ANDA", "marketing_start_date": "20220926", "listing_expiration_date": "20261231"}