diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler apotex corp.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 180 mg/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-0015
Product ID 60505-0015_e06c5d5f-878e-6bb1-793c-642751592404
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074943
Listing Expiration 2026-12-31
Marketing Start 2001-07-30

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 605050015
Hyphenated Format 60505-0015

Supplemental Identifiers

RxCUI
830837 830845 830861 831215 831252 831285
UPC
0360505001460 0360505001569
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 diltiazem hydrochloride (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number ANDA074943 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0015-6)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0015-8)
source: ndc

Packages (2)

60505-0015-6 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0015-6) 60505-0015-8 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0015-8)

Ingredients (1)

diltiazem hydrochloride (180 mg/1)

Linked Drug Pages (1)

DILTIAZEM HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e06c5d5f-878e-6bb1-793c-642751592404", "openfda": {"upc": ["0360505001460", "0360505001569"], "unii": ["OLH94387TE"], "rxcui": ["830837", "830845", "830861", "831215", "831252", "831285"], "spl_set_id": ["56573e9d-7bd2-694c-cd6d-26039590e548"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0015-8)", "package_ndc": "60505-0015-8", "marketing_start_date": "20010730"}, {"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0015-6)", "package_ndc": "60505-0015-6", "marketing_start_date": "20010730"}], "brand_name": "DILTIAZEM HYDROCHLORIDE", "product_id": "60505-0015_e06c5d5f-878e-6bb1-793c-642751592404", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "60505-0015", "generic_name": "DILTIAZEM HYDROCHLORIDE", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DILTIAZEM HYDROCHLORIDE", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA074943", "marketing_category": "ANDA", "marketing_start_date": "20010730", "listing_expiration_date": "20261231"}