cartia xt

Generic: diltiazem hydrochloride

Labeler: directrx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cartia xt
Generic Name diltiazem hydrochloride
Labeler directrx
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 300 mg/1

Manufacturer
DirectRx

Identifiers & Regulatory

Product NDC 72189-344
Product ID 72189-344_2c4c7b35-cdc7-a9c1-e063-6394a90a7634
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074752
Listing Expiration 2026-12-31
Marketing Start 2022-04-06

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 72189344
Hyphenated Format 72189-344

Supplemental Identifiers

UNII
OLH94387TE

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
  • 300 mg/1
source: ndc
Packaging
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-344-90)
source: ndc

Packages (1)

Ingredients (1)

diltiazem hydrochloride (300 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4c7b35-cdc7-a9c1-e063-6394a90a7634", "openfda": {"unii": ["OLH94387TE"], "spl_set_id": ["dbfda3a5-5602-6e47-e053-2995a90ac07b"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-344-90)", "package_ndc": "72189-344-90", "marketing_start_date": "20220406"}], "brand_name": "CARTIA XT", "product_id": "72189-344_2c4c7b35-cdc7-a9c1-e063-6394a90a7634", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "72189-344", "generic_name": "diltiazem hydrochloride", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARTIA XT", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA074752", "marketing_category": "ANDA", "marketing_start_date": "20220406", "listing_expiration_date": "20261231"}