diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 120 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4242
Product ID 68071-4242_1a3c5c49-b375-1318-e063-6394a90a47b6
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] cytochrome p450 3a4 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680714242
Hyphenated Format 68071-4242

Supplemental Identifiers

RxCUI
831054
UPC
0368071424232
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 diltiazem hydrochloride (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number NDA018602 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-4242-3)
source: ndc

Packages (1)

68071-4242-3 30 TABLET in 1 BOTTLE (68071-4242-3)

Ingredients (1)

diltiazem hydrochloride (120 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": "1a3c5c49-b375-1318-e063-6394a90a47b6", "openfda": {"upc": ["0368071424232"], "unii": ["OLH94387TE"], "rxcui": ["831054"], "spl_set_id": ["636556f6-2987-984f-e053-2991aa0a201a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4242-3)", "package_ndc": "68071-4242-3", "marketing_start_date": "20180122"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "68071-4242_1a3c5c49-b375-1318-e063-6394a90a47b6", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "68071-4242", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "NDA018602", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}