Package 72189-409-90
Brand: diltiazem hcl er
Generic: diltiazem hcl erPackage Facts
Identity
Package NDC
72189-409-90
Digits Only
7218940990
Product NDC
72189-409
Description
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-409-90)
Marketing
Marketing Status
Brand
diltiazem hcl er
Generic
diltiazem hcl er
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4ce2c4-2b19-de10-e063-6394a90ad371", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830801"], "spl_set_id": ["f1ea85b2-ecd2-5867-e053-2a95a90a24dc"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-409-90)", "package_ndc": "72189-409-90", "marketing_start_date": "20230110"}], "brand_name": "Diltiazem HCL ER", "product_id": "72189-409_2c4ce2c4-2b19-de10-e063-6394a90ad371", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "72189-409", "generic_name": "Diltiazem HCL ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem HCL ER", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA208783", "marketing_category": "ANDA", "marketing_start_date": "20230110", "listing_expiration_date": "20261231"}