verapamil hydrochloride

Generic: verapamil hydrochloride

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

Drug Facts

Product Profile

Brand Name verapamil hydrochloride
Generic Name verapamil hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

verapamil hydrochloride 120 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8696
Product ID 68788-8696_dfb38dc3-25c5-472c-b723-c407be886316
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206173
Listing Expiration 2026-12-31
Marketing Start 2024-06-11

Pharmacologic Class

Classes
calcium channel antagonists [moa] calcium channel blocker [epc] cytochrome p450 3a inhibitors [moa] cytochrome p450 3a4 inhibitors [moa] p-glycoprotein inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888696
Hyphenated Format 68788-8696

Supplemental Identifiers

RxCUI
897659
UNII
V3888OEY5R

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 verapamil hydrochloride (source: ndc)
Generic Name verapamil hydrochloride (source: ndc)
Application Number ANDA206173 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-8696-1)
  • 30 TABLET in 1 BOTTLE (68788-8696-3)
  • 90 TABLET in 1 BOTTLE (68788-8696-9)
source: ndc

Packages (3)

68788-8696-1 100 TABLET in 1 BOTTLE (68788-8696-1) 68788-8696-3 30 TABLET in 1 BOTTLE (68788-8696-3) 68788-8696-9 90 TABLET in 1 BOTTLE (68788-8696-9)

Ingredients (1)

verapamil hydrochloride (120 mg/1)

Linked Drug Pages (1)

VERAPAMIL HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dfb38dc3-25c5-472c-b723-c407be886316", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897659"], "spl_set_id": ["b0eeada4-1010-4c11-b408-29f9a1af23c0"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8696-1)", "package_ndc": "68788-8696-1", "marketing_start_date": "20240611"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8696-3)", "package_ndc": "68788-8696-3", "marketing_start_date": "20240611"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8696-9)", "package_ndc": "68788-8696-9", "marketing_start_date": "20240611"}], "brand_name": "VERAPAMIL HYDROCHLORIDE", "product_id": "68788-8696_dfb38dc3-25c5-472c-b723-c407be886316", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "68788-8696", "generic_name": "VERAPAMIL HYDROCHLORIDE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VERAPAMIL HYDROCHLORIDE", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA206173", "marketing_category": "ANDA", "marketing_start_date": "20240611", "listing_expiration_date": "20261231"}