diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: oceanside pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
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 68682-998
Product ID 68682-998_c44f803b-1698-4e4f-845f-ae0f54c9d121
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075116
Listing Expiration 2026-12-31
Marketing Start 1999-12-28

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 68682998
Hyphenated Format 68682-998

Supplemental Identifiers

RxCUI
830801 830837 830845 830861
UPC
0368682993981
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 ANDA075116 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68682-998-98)
source: ndc

Packages (1)

68682-998-98 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68682-998-98)

Ingredients (1)

diltiazem hydrochloride (300 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": "c44f803b-1698-4e4f-845f-ae0f54c9d121", "openfda": {"upc": ["0368682993981"], "unii": ["OLH94387TE"], "rxcui": ["830801", "830837", "830845", "830861"], "spl_set_id": ["43892b97-449d-45bc-bb09-29d47c655d65"], "manufacturer_name": ["OCEANSIDE PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68682-998-98)", "package_ndc": "68682-998-98", "marketing_start_date": "19991228"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "68682-998_c44f803b-1698-4e4f-845f-ae0f54c9d121", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "68682-998", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "OCEANSIDE PHARMACEUTICALS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA075116", "marketing_category": "ANDA", "marketing_start_date": "19991228", "listing_expiration_date": "20261231"}