Package 71872-7293-1
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
71872-7293-1
Digits Only
7187272931
Product NDC
71872-7293
Description
1 VIAL in 1 BAG (71872-7293-1) / 5 mL in 1 VIAL
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": ["INTRAVENOUS"], "spl_id": "fbd7e438-7ad1-86cc-e053-6394a90aa9d2", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["1791229"], "spl_set_id": ["fbd7ee32-fabe-06e7-e053-6294a90a63e0"], "manufacturer_name": ["Medical Purchasing Solutions, LLC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7293-1) / 5 mL in 1 VIAL", "package_ndc": "71872-7293-1", "marketing_start_date": "20230417"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "71872-7293_fbd7e438-7ad1-86cc-e053-6394a90aa9d2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71872-7293", "generic_name": "diltiazem hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA074617", "marketing_category": "ANDA", "marketing_start_date": "20191215", "listing_expiration_date": "20261231"}