diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

diltiazem hydrochloride 30 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-3659
Product ID 63629-3659_c0d753f2-73e1-42a6-92c2-35718c3e53a6
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 636293659
Hyphenated Format 63629-3659

Supplemental Identifiers

RxCUI
833217
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 ANDA074185 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (63629-3659-1)
source: ndc

Packages (1)

63629-3659-1 90 TABLET, FILM COATED in 1 BOTTLE (63629-3659-1)

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": "c0d753f2-73e1-42a6-92c2-35718c3e53a6", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["833217"], "spl_set_id": ["6ca6a648-fc67-4cf8-a1f7-787c9574e3a1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-3659-1)", "package_ndc": "63629-3659-1", "marketing_start_date": "20240327"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "63629-3659_c0d753f2-73e1-42a6-92c2-35718c3e53a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "63629-3659", "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": "30 mg/1"}], "application_number": "ANDA074185", "marketing_category": "ANDA", "marketing_start_date": "19951222", "listing_expiration_date": "20261231"}