Package 50090-7401-2

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7401-2
Digits Only 5009074012
Product NDC 50090-7401
Description

30 TABLET in 1 BOTTLE (50090-7401-2)

Marketing

Marketing Status
Marketed Since 2024-10-24
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": "a00809e7-b922-47f3-823f-e2fe07d0c260", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["831103"], "spl_set_id": ["88b150a6-4c8d-49c8-88df-f3606c335472"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7401-2)", "package_ndc": "50090-7401-2", "marketing_start_date": "20241024"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7401-3)", "package_ndc": "50090-7401-3", "marketing_start_date": "20241024"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "50090-7401_a00809e7-b922-47f3-823f-e2fe07d0c260", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "50090-7401", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA216521", "marketing_category": "ANDA", "marketing_start_date": "20220926", "listing_expiration_date": "20261231"}