verapamil hydrochloride

Generic: verapamil hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name verapamil hydrochloride
Generic Name verapamil hydrochloride
Labeler actavis pharma, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

verapamil hydrochloride 40 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-0404
Product ID 0591-0404_98d6e01a-d15c-47b4-82ae-87705e8ed7a9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072924
Listing Expiration 2026-12-31
Marketing Start 1993-06-29

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 05910404
Hyphenated Format 0591-0404

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 ANDA072924 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0404-01)
source: ndc

Packages (1)

0591-0404-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0404-01)

Ingredients (1)

verapamil hydrochloride (40 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": "98d6e01a-d15c-47b4-82ae-87705e8ed7a9", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897666", "897683", "897722"], "spl_set_id": ["a0343397-897b-46d6-943f-a87e07e1de10"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0404-01)", "package_ndc": "0591-0404-01", "marketing_start_date": "19930629"}], "brand_name": "Verapamil Hydrochloride", "product_id": "0591-0404_98d6e01a-d15c-47b4-82ae-87705e8ed7a9", "dosage_form": "TABLET, FILM COATED", "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": "0591-0404", "generic_name": "Verapamil Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Verapamil Hydrochloride", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA072924", "marketing_category": "ANDA", "marketing_start_date": "19930629", "listing_expiration_date": "20261231"}