cartia xt

Generic: diltiazem hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cartia xt
Generic Name diltiazem hydrochloride
Labeler actavis pharma, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 180 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 62037-598
Product ID 62037-598_3bd8ffd9-1836-46a3-bf34-624b27d0973c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074752
Listing Expiration 2026-12-31
Marketing Start 1998-07-09

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 62037598
Hyphenated Format 62037-598

Supplemental Identifiers

RxCUI
830801 830837 830845 830861 831226 831255 831309 831338
UPC
0362037598906 0362037599903 0362037597909 0362037600906
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 cartia xt (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number ANDA074752 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-05)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-90)
source: ndc

Packages (2)

62037-598-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-05) 62037-598-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-90)

Ingredients (1)

diltiazem hydrochloride (180 mg/1)

Linked Drug Pages (1)

Cartia XT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3bd8ffd9-1836-46a3-bf34-624b27d0973c", "openfda": {"upc": ["0362037598906", "0362037599903", "0362037597909", "0362037600906"], "unii": ["OLH94387TE"], "rxcui": ["830801", "830837", "830845", "830861", "831226", "831255", "831309", "831338"], "spl_set_id": ["2dc2b889-8443-4f7f-83be-86c68e179804"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-05)", "package_ndc": "62037-598-05", "marketing_start_date": "19990623"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-90)", "package_ndc": "62037-598-90", "marketing_start_date": "19990623"}], "brand_name": "Cartia XT", "product_id": "62037-598_3bd8ffd9-1836-46a3-bf34-624b27d0973c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "62037-598", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cartia", "brand_name_suffix": "XT", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA074752", "marketing_category": "ANDA", "marketing_start_date": "19980709", "listing_expiration_date": "20261231"}