diltiazem hydrochloride extended release

Generic: diltiazem hydrochloride

Labeler: oceanside pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride extended release
Generic Name diltiazem hydrochloride
Labeler oceanside pharmaceuticals
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 300 mg/1

Manufacturer
Oceanside Pharmaceuticals

Identifiers & Regulatory

Product NDC 68682-370
Product ID 68682-370_f51e2ce0-22dd-4a31-bab8-70b0b55864af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020401
Listing Expiration 2026-12-31
Marketing Start 2014-08-20

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 68682370
Hyphenated Format 68682-370

Supplemental Identifiers

RxCUI
830795 830801 830837 830845 830861 831359
UPC
0368682369908
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 extended release (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number NDA020401 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68682-370-90)
source: ndc

Packages (1)

68682-370-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68682-370-90)

Ingredients (1)

diltiazem hydrochloride (300 mg/1)

Linked Drug Pages (1)

Diltiazem Hydrochloride EXTENDED RELEASE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f51e2ce0-22dd-4a31-bab8-70b0b55864af", "openfda": {"upc": ["0368682369908"], "unii": ["OLH94387TE"], "rxcui": ["830795", "830801", "830837", "830845", "830861", "831359"], "spl_set_id": ["862d65cb-a732-4786-b569-bad2eaafddfd"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68682-370-90)", "package_ndc": "68682-370-90", "marketing_start_date": "20140820"}], "brand_name": "Diltiazem Hydrochloride EXTENDED RELEASE", "product_id": "68682-370_f51e2ce0-22dd-4a31-bab8-70b0b55864af", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "68682-370", "generic_name": "diltiazem hydrochloride", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "brand_name_suffix": "EXTENDED RELEASE", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "NDA020401", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}