diltiazem hydrochloride extended release

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 extended release
Generic Name diltiazem hydrochloride
Labeler bryant ranch prepack
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 240 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1585
Product ID 71335-1585_9308bc71-ce3f-429f-9926-d140481ad8ab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020401
Listing Expiration 2026-12-31
Marketing Start 2014-08-20

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 713351585
Hyphenated Format 71335-1585

Supplemental Identifiers

RxCUI
830837
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 extended release (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number NDA020401 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 240 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-1)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-2)
  • 18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-3)
source: ndc

Packages (3)

71335-1585-1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-1) 71335-1585-2 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-2) 71335-1585-3 18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-3)

Ingredients (1)

diltiazem hydrochloride (240 mg/1)

Linked Drug Pages (1)

Diltiazem Hydrochloride EXTENDED RELEASE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9308bc71-ce3f-429f-9926-d140481ad8ab", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830837"], "spl_set_id": ["c7c6a74e-5f73-4265-a0e0-8fd2cd26909e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-1)", "package_ndc": "71335-1585-1", "marketing_start_date": "20220211"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-2)", "package_ndc": "71335-1585-2", "marketing_start_date": "20220211"}, {"sample": false, "description": "18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-3)", "package_ndc": "71335-1585-3", "marketing_start_date": "20220211"}], "brand_name": "Diltiazem Hydrochloride EXTENDED RELEASE", "product_id": "71335-1585_9308bc71-ce3f-429f-9926-d140481ad8ab", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71335-1585", "generic_name": "diltiazem hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "brand_name_suffix": "EXTENDED RELEASE", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "NDA020401", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}