Package 0093-0320-01

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-0320-01
Digits Only 0093032001
Product NDC 0093-0320
Product ID 0093-0320_eb4d8470-1f38-42c6-a511-8383066ed454
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-0320-01)

Marketing

Marketing Status
Marketed Since 1995-12-22
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": "eb4d8470-1f38-42c6-a511-8383066ed454", "openfda": {"upc": ["0300930319013", "0300930320019", "0300930321016"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831102", "831103", "833217"], "spl_set_id": ["69ca7cae-fdf3-413a-900b-95cf6e9e7b63"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0320-01)", "package_ndc": "0093-0320-01", "marketing_start_date": "19951222"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "0093-0320_eb4d8470-1f38-42c6-a511-8383066ed454", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0093-0320", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA074185", "marketing_category": "ANDA", "marketing_start_date": "19951222", "listing_expiration_date": "20261231"}