diltiazem hydrochloride

Generic: diltiazem hydrochloride

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

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler oceanside pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 30 mg/1

Manufacturer
Oceanside Pharmaceuticals

Identifiers & Regulatory

Product NDC 68682-006
Product ID 68682-006_06626a5d-987f-4d1c-9ffc-28fd51362900
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018602
Listing Expiration 2026-12-31
Marketing Start 2010-12-25

Pharmacologic Class

Classes
calcium channel antagonists [moa] calcium channel blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68682006
Hyphenated Format 68682-006

Supplemental Identifiers

RxCUI
831054 831102 831103 833217
UPC
0368682006100 0368682009101 0368682008104 0368682007107
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 NDA018602 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68682-006-10)
  • 500 TABLET in 1 BOTTLE (68682-006-50)
source: ndc

Packages (2)

68682-006-10 100 TABLET in 1 BOTTLE (68682-006-10) 68682-006-50 500 TABLET in 1 BOTTLE (68682-006-50)

Ingredients (1)

diltiazem hydrochloride (30 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": "06626a5d-987f-4d1c-9ffc-28fd51362900", "openfda": {"upc": ["0368682006100", "0368682009101", "0368682008104", "0368682007107"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831102", "831103", "833217"], "spl_set_id": ["f6a24de7-8ffe-48af-873f-10fdcd5551d1"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68682-006-10)", "package_ndc": "68682-006-10", "marketing_start_date": "20101225"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68682-006-50)", "package_ndc": "68682-006-50", "marketing_start_date": "20101225"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "68682-006_06626a5d-987f-4d1c-9ffc-28fd51362900", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]"], "product_ndc": "68682-006", "generic_name": "Diltiazem hydrochloride", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA018602", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}