Package 51662-1335-1
Brand: diltiazem hci
Generic: diltiazem hciPackage Facts
Identity
Package NDC
51662-1335-1
Digits Only
5166213351
Product NDC
51662-1335
Description
5 mL in 1 VIAL (51662-1335-1)
Marketing
Marketing Status
Brand
diltiazem hci
Generic
diltiazem hci
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f2a0ac76-9d93-eaad-e053-2a95a90a4d67", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["1791229"], "spl_set_id": ["7d8e8b1e-f67b-57d2-e053-2991aa0a8d12"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL (51662-1335-1)", "package_ndc": "51662-1335-1", "marketing_start_date": "20181221"}, {"sample": false, "description": "1 VIAL in 1 POUCH (51662-1335-2) / 5 mL in 1 VIAL", "package_ndc": "51662-1335-2", "marketing_start_date": "20230119"}], "brand_name": "DILTIAZEM HCI", "product_id": "51662-1335_f2a0ac76-9d93-eaad-e053-2a95a90a4d67", "dosage_form": "INJECTION", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]"], "product_ndc": "51662-1335", "generic_name": "DILTIAZEM HCI", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DILTIAZEM HCI", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA078538", "marketing_category": "ANDA", "marketing_start_date": "20181221", "listing_expiration_date": "20261231"}