cardizem la

Generic: diltiazem hydrochloride

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

Drug Facts

Product Profile

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

diltiazem hydrochloride 360 mg/1

Manufacturer
Bausch Health US LLC

Identifiers & Regulatory

Product NDC 0187-2049
Product ID 0187-2049_1771fff3-92c3-48ee-b786-5d6d7c6e6628
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021392
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 01872049
Hyphenated Format 0187-2049

Supplemental Identifiers

RxCUI
830874 830876 830877 830878 830879 830880 830882 830883 830897 830898 830900 830902
UPC
0301872045909 0301872047903
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 la (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number NDA021392 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 360 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-90)
source: ndc

Packages (2)

0187-2049-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-30) 0187-2049-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-90)

Ingredients (1)

diltiazem hydrochloride (360 mg/1)

Linked Drug Pages (1)

Cardizem LA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1771fff3-92c3-48ee-b786-5d6d7c6e6628", "openfda": {"upc": ["0301872045909", "0301872047903"], "unii": ["OLH94387TE"], "rxcui": ["830874", "830876", "830877", "830878", "830879", "830880", "830882", "830883", "830897", "830898", "830900", "830902"], "spl_set_id": ["3e180dc7-c871-4efc-8755-cae882976c8d"], "manufacturer_name": ["Bausch Health US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-30)", "package_ndc": "0187-2049-30", "marketing_start_date": "20101225"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-90)", "package_ndc": "0187-2049-90", "marketing_start_date": "20101225"}], "brand_name": "Cardizem LA", "product_id": "0187-2049_1771fff3-92c3-48ee-b786-5d6d7c6e6628", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0187-2049", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bausch Health US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cardizem LA", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "360 mg/1"}], "application_number": "NDA021392", "marketing_category": "NDA", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}