diltiazem hydrochloride
Generic: diltiazem hydrochloride
Labeler: upsher-smith laboratories, llcDrug Facts
Product Profile
Brand Name
diltiazem hydrochloride
Generic Name
diltiazem hydrochloride
Labeler
upsher-smith laboratories, llc
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
diltiazem hydrochloride 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
24979-181
Product ID
24979-181_515b321d-2983-49dd-bccd-4e4e375e33c0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217377
Listing Expiration
2026-12-31
Marketing Start
2023-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24979181
Hyphenated Format
24979-181
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA217377 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
Packaging
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-181-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "515b321d-2983-49dd-bccd-4e4e375e33c0", "openfda": {"upc": ["0324979183015", "0324979182018", "0324979181011"], "unii": ["OLH94387TE"], "rxcui": ["830865", "830869", "830872"], "spl_set_id": ["f276d9fe-a685-4d99-ad82-d4452ef4ba98"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-181-01)", "package_ndc": "24979-181-01", "marketing_start_date": "20230501"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "24979-181_515b321d-2983-49dd-bccd-4e4e375e33c0", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "24979-181", "generic_name": "diltiazem hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA217377", "marketing_category": "ANDA", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}