verapamil hydrochloride

Generic: verapamil hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name verapamil hydrochloride
Generic Name verapamil hydrochloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

verapamil hydrochloride 120 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-486
Product ID 23155-486_751ba5e8-14b3-4fdb-8e8e-ca59867fd257
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071881
Listing Expiration 2026-12-31
Marketing Start 2018-07-20

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 23155486
Hyphenated Format 23155-486

Supplemental Identifiers

RxCUI
897666 897683 897722
UNII
V3888OEY5R

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 verapamil hydrochloride (source: ndc)
Generic Name verapamil hydrochloride (source: ndc)
Application Number ANDA071881 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-486-01)
  • 500 TABLET in 1 BOTTLE (23155-486-05)
source: ndc

Packages (2)

23155-486-01 100 TABLET in 1 BOTTLE (23155-486-01) 23155-486-05 500 TABLET in 1 BOTTLE (23155-486-05)

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": "751ba5e8-14b3-4fdb-8e8e-ca59867fd257", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897666", "897683", "897722"], "spl_set_id": ["ed1e0c14-3571-43f9-88fc-5a4d2b598263"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-486-01)", "package_ndc": "23155-486-01", "marketing_start_date": "20180720"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-486-05)", "package_ndc": "23155-486-05", "marketing_start_date": "20180720"}], "brand_name": "VERAPAMIL HYDROCHLORIDE", "product_id": "23155-486_751ba5e8-14b3-4fdb-8e8e-ca59867fd257", "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": "23155-486", "generic_name": "VERAPAMIL HYDROCHLORIDE", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VERAPAMIL HYDROCHLORIDE", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA071881", "marketing_category": "ANDA", "marketing_start_date": "20180720", "listing_expiration_date": "20261231"}