diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 30 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-036
Product ID 82868-036_47f89c58-08d5-61d7-e063-6394a90a39a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216521
Listing Expiration 2027-12-31
Marketing Start 2024-01-18

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 82868036
Hyphenated Format 82868-036

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 ANDA216521 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE, PLASTIC (82868-036-10)
source: ndc

Packages (1)

82868-036-10 10 TABLET in 1 BOTTLE, PLASTIC (82868-036-10)

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": "47f89c58-08d5-61d7-e063-6394a90a39a2", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["833217"], "spl_set_id": ["106b33e3-b199-e555-e063-6294a90a5af5"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (82868-036-10)", "package_ndc": "82868-036-10", "marketing_start_date": "20240118"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "82868-036_47f89c58-08d5-61d7-e063-6394a90a39a2", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "82868-036", "generic_name": "Diltiazem hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA216521", "marketing_category": "ANDA", "marketing_start_date": "20240118", "listing_expiration_date": "20271231"}