Package 70436-199-04
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
70436-199-04
Digits Only
7043619904
Product NDC
70436-199
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-199-04)
Marketing
Marketing Status
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": "44e0c7a1-c1bd-41e2-e063-6294a90a969d", "openfda": {"upc": ["0370436199068", "0370436196067", "0370436200047", "0370436197064", "0370436197040", "0370436198047", "0370436200061", "0370436198061", "0370436199044", "0370436195046", "0370436195060", "0370436196043"], "unii": ["OLH94387TE"], "rxcui": ["830874", "830877", "830879", "830882", "830897", "830900"], "spl_set_id": ["f7137458-0db3-7ecd-e053-6394a90a5f95"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-199-04)", "package_ndc": "70436-199-04", "marketing_start_date": "20230320"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-199-06)", "package_ndc": "70436-199-06", "marketing_start_date": "20230320"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "70436-199_44e0c7a1-c1bd-41e2-e063-6294a90a969d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "70436-199", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "360 mg/1"}], "application_number": "ANDA216439", "marketing_category": "ANDA", "marketing_start_date": "20230320", "listing_expiration_date": "20261231"}