diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 90 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0579
Product ID 71335-0579_fd901e8d-53ca-6e15-e053-6294a90a4b31
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 713350579
Hyphenated Format 71335-0579

Supplemental Identifiers

RxCUI
831102
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
  • 90 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0579-1)
  • 90 TABLET in 1 BOTTLE (71335-0579-2)
source: ndc

Packages (2)

71335-0579-1 30 TABLET in 1 BOTTLE (71335-0579-1) 71335-0579-2 90 TABLET in 1 BOTTLE (71335-0579-2)

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": "fd901e8d-53ca-6e15-e053-6294a90a4b31", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["831102"], "spl_set_id": ["225a87fb-d353-4ee7-bd08-14d631ff6b16"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0579-1)", "package_ndc": "71335-0579-1", "marketing_start_date": "20211227"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0579-2)", "package_ndc": "71335-0579-2", "marketing_start_date": "20180313"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "71335-0579_fd901e8d-53ca-6e15-e053-6294a90a4b31", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71335-0579", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "NDA018602", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20101225", "listing_expiration_date": "20261231"}