cardizem

Generic: diltiazem hydrochloride

Labeler: bausch health us llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cardizem
Generic Name diltiazem hydrochloride
Labeler bausch health us llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 60 mg/1

Manufacturer
Bausch Health US LLC

Identifiers & Regulatory

Product NDC 0187-0772
Product ID 0187-0772_340462fa-5523-448e-e063-6294a90a4eab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018602
Listing Expiration 2026-12-31
Marketing Start 2010-12-25

Pharmacologic Class

Classes
calcium channel antagonists [moa] calcium channel blocker [epc] cytochrome p450 3a4 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01870772
Hyphenated Format 0187-0772

Supplemental Identifiers

RxCUI
831054 831055 831102 831103 831137 833217 833219 834393
UPC
0301870772470 0301870791471 0301870792478 0301870771473
UNII
OLH94387TE

Packaging Origin

Original Packager
true

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 cardizem (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number NDA018602 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (0187-0772-47)
source: ndc

Packages (1)

0187-0772-47 100 TABLET, COATED in 1 BOTTLE (0187-0772-47)

Ingredients (1)

diltiazem hydrochloride (60 mg/1)

Linked Drug Pages (1)

Cardizem ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "340462fa-5523-448e-e063-6294a90a4eab", "openfda": {"upc": ["0301870772470", "0301870791471", "0301870792478", "0301870771473"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831055", "831102", "831103", "831137", "833217", "833219", "834393"], "spl_set_id": ["f3e7ecef-f360-4987-a4f5-933214130ab2"], "manufacturer_name": ["Bausch Health US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (0187-0772-47)", "package_ndc": "0187-0772-47", "marketing_start_date": "20101225"}], "brand_name": "Cardizem", "product_id": "0187-0772_340462fa-5523-448e-e063-6294a90a4eab", "dosage_form": "TABLET, COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0187-0772", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bausch Health US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cardizem", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "NDA018602", "marketing_category": "NDA", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}