diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 90 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0320
Product ID 0093-0320_eb4d8470-1f38-42c6-a511-8383066ed454
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074185
Listing Expiration 2026-12-31
Marketing Start 1995-12-22

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 00930320
Hyphenated Format 0093-0320

Supplemental Identifiers

RxCUI
831054 831102 831103 833217
UPC
0300930319013 0300930320019 0300930321016
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 ANDA074185 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 90 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0093-0320-01)
source: ndc

Packages (1)

0093-0320-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-0320-01)

Ingredients (1)

diltiazem hydrochloride (90 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": "eb4d8470-1f38-42c6-a511-8383066ed454", "openfda": {"upc": ["0300930319013", "0300930320019", "0300930321016"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831102", "831103", "833217"], "spl_set_id": ["69ca7cae-fdf3-413a-900b-95cf6e9e7b63"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0320-01)", "package_ndc": "0093-0320-01", "marketing_start_date": "19951222"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "0093-0320_eb4d8470-1f38-42c6-a511-8383066ed454", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "0093-0320", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA074185", "marketing_category": "ANDA", "marketing_start_date": "19951222", "listing_expiration_date": "20261231"}