Package 60687-717-01
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
60687-717-01
Digits Only
6068771701
Product NDC
60687-717
Description
100 BLISTER PACK in 1 CARTON (60687-717-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-717-11)
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": "437e5fb1-aebc-9dd7-e063-6294a90ad921", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["831103", "833217"], "spl_set_id": ["14869f9e-6a66-4f75-b0fc-4d808b1ee85e"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-717-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-717-11)", "package_ndc": "60687-717-01", "marketing_start_date": "20230327"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "60687-717_437e5fb1-aebc-9dd7-e063-6294a90ad921", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "60687-717", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA074185", "marketing_category": "ANDA", "marketing_start_date": "20230327", "listing_expiration_date": "20261231"}