verapamil hydrochloride

Generic: verapamil hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name verapamil hydrochloride
Generic Name verapamil hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

verapamil hydrochloride 120 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-849
Product ID 63187-849_0e9c3eb8-1ae1-45b3-8304-10dc0a3c9b4d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090700
Listing Expiration 2026-12-31
Marketing Start 2011-08-05

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 63187849
Hyphenated Format 63187-849

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 ANDA090700 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-30)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-60)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-90)
source: ndc

Packages (3)

Ingredients (1)

verapamil hydrochloride (120 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e9c3eb8-1ae1-45b3-8304-10dc0a3c9b4d", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897659"], "spl_set_id": ["19cb23bd-cc6d-45fc-a1fc-b4130ea460a6"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-30)", "package_ndc": "63187-849-30", "marketing_start_date": "20110805"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-60)", "package_ndc": "63187-849-60", "marketing_start_date": "20110805"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-90)", "package_ndc": "63187-849-90", "marketing_start_date": "20110805"}], "brand_name": "verapamil hydrochloride", "product_id": "63187-849_0e9c3eb8-1ae1-45b3-8304-10dc0a3c9b4d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "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": "63187-849", "generic_name": "verapamil hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "verapamil hydrochloride", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090700", "marketing_category": "ANDA", "marketing_start_date": "20110805", "listing_expiration_date": "20261231"}