cartia xt

Generic: diltiazem hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

diltiazem hydrochloride 180 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0879
Product ID 71335-0879_053455c6-3889-4a52-9981-db90a6bce8ed
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 713350879
Hyphenated Format 71335-0879

Supplemental Identifiers

RxCUI
830845 831255
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
  • 180 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-1)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-2)
source: ndc

Packages (2)

71335-0879-1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-1) 71335-0879-2 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-2)

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": "053455c6-3889-4a52-9981-db90a6bce8ed", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830845", "831255"], "spl_set_id": ["e02f5fad-6482-4d5d-91c5-0ae6b0ce15b8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-1)", "package_ndc": "71335-0879-1", "marketing_start_date": "20180625"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-2)", "package_ndc": "71335-0879-2", "marketing_start_date": "20211227"}], "brand_name": "Cartia XT", "product_id": "71335-0879_053455c6-3889-4a52-9981-db90a6bce8ed", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71335-0879", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}