diltiazem hydrochloride
Generic: diltiazem hydrochloride
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
diltiazem hydrochloride
Generic Name
diltiazem hydrochloride
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
diltiazem hydrochloride 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82868-024
Product ID
82868-024_47fc4881-8e2e-0e98-e063-6294a90af6d2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216521
Listing Expiration
2027-12-31
Marketing Start
2023-11-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82868024
Hyphenated Format
82868-024
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
diltiazem hydrochloride (source: ndc)
Generic Name
diltiazem hydrochloride (source: ndc)
Application Number
ANDA216521 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (82868-024-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47fc4881-8e2e-0e98-e063-6294a90af6d2", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["831103"], "spl_set_id": ["09a5d332-347b-e73d-e063-6294a90a67ed"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-024-30)", "package_ndc": "82868-024-30", "marketing_start_date": "20231103"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "82868-024_47fc4881-8e2e-0e98-e063-6294a90af6d2", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "82868-024", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA216521", "marketing_category": "ANDA", "marketing_start_date": "20231103", "listing_expiration_date": "20271231"}