Package 68682-009-10

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68682-009-10
Digits Only 6868200910
Product NDC 68682-009
Product ID 68682-009_06626a5d-987f-4d1c-9ffc-28fd51362900
Description

100 TABLET in 1 BOTTLE (68682-009-10)

Marketing

Marketing Status
Marketed Since 2010-12-25
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": "06626a5d-987f-4d1c-9ffc-28fd51362900", "openfda": {"upc": ["0368682006100", "0368682009101", "0368682008104", "0368682007107"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831102", "831103", "833217"], "spl_set_id": ["f6a24de7-8ffe-48af-873f-10fdcd5551d1"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68682-009-10)", "package_ndc": "68682-009-10", "marketing_start_date": "20101225"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "68682-009_06626a5d-987f-4d1c-9ffc-28fd51362900", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]"], "product_ndc": "68682-009", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "NDA018602", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}