Package 62135-335-90

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-335-90
Digits Only 6213533590
Product NDC 62135-335
Description

90 TABLET in 1 BOTTLE (62135-335-90)

Marketing

Marketing Status
Marketed Since 2024-06-17
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": "1b432d9d-b46c-2ee8-e063-6294a90adb54", "openfda": {"upc": ["0362135334123", "0362135336905", "0362135335908", "0362135333126"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831102", "831103", "833217"], "spl_set_id": ["51abce7b-e3d1-44b5-bccc-d463150d0bba"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-335-90)", "package_ndc": "62135-335-90", "marketing_start_date": "20240617"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "62135-335_1b432d9d-b46c-2ee8-e063-6294a90adb54", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "62135-335", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA074093", "marketing_category": "ANDA", "marketing_start_date": "19921105", "listing_expiration_date": "20261231"}