diltiazem hydrochloride
Generic: diltiazem hydrochloride
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
diltiazem hydrochloride
Generic Name
diltiazem hydrochloride
Labeler
cardinal health 107, llc
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
diltiazem hydrochloride 240 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55154-2627
Product ID
55154-2627_fec71967-874e-45ef-b08f-54da70096457
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205231
Listing Expiration
2026-12-31
Marketing Start
2023-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551542627
Hyphenated Format
55154-2627
Supplemental Identifiers
RxCUI
UPC
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
ANDA205231 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 240 mg/1
Packaging
- 10 BLISTER PACK in 1 BAG (55154-2627-0) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fec71967-874e-45ef-b08f-54da70096457", "openfda": {"upc": ["0055154432108", "0055154262705", "0055154431705"], "unii": ["OLH94387TE"], "rxcui": ["830837", "830845", "830861"], "spl_set_id": ["bdb9e7cf-bfbb-48b4-a8be-9038820d8279"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2627-0) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-2627-0", "marketing_start_date": "20230801"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "55154-2627_fec71967-874e-45ef-b08f-54da70096457", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "55154-2627", "generic_name": "Diltiazem hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "ANDA205231", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}