diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler alembic pharmaceuticals inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 240 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-727
Product ID 62332-727_3e0914c5-051a-45fb-868f-3359e9ba76e7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216968
Listing Expiration 2026-12-31
Marketing Start 2024-11-14

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 62332727
Hyphenated Format 62332-727

Supplemental Identifiers

RxCUI
830795 830801 830837 830845 830861
UPC
0362332727308 0362332729302 0362332725304 0362332728305 0362332726301
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 ANDA216968 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 240 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-727-30)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-727-90)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-727-91)
source: ndc

Packages (3)

Ingredients (1)

diltiazem hydrochloride (240 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e0914c5-051a-45fb-868f-3359e9ba76e7", "openfda": {"upc": ["0362332727308", "0362332729302", "0362332725304", "0362332728305", "0362332726301"], "unii": ["OLH94387TE"], "rxcui": ["830795", "830801", "830837", "830845", "830861"], "spl_set_id": ["ac9aa10d-cd52-4ac9-a01d-e3cbf14d4913"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-727-30)", "package_ndc": "62332-727-30", "marketing_start_date": "20241114"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-727-90)", "package_ndc": "62332-727-90", "marketing_start_date": "20241114"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-727-91)", "package_ndc": "62332-727-91", "marketing_start_date": "20241114"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "62332-727_3e0914c5-051a-45fb-868f-3359e9ba76e7", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "62332-727", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "ANDA216968", "marketing_category": "ANDA", "marketing_start_date": "20241114", "listing_expiration_date": "20261231"}