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
Routes
ORAL
Active Ingredients

verapamil hydrochloride 120 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-129
Product ID 71205-129_3bdf016f-4176-4fd8-aae5-c0806d80daee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070994
Listing Expiration 2026-12-31
Marketing Start 1986-10-01

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 71205129
Hyphenated Format 71205-129

Supplemental Identifiers

RxCUI
897666
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 ANDA070994 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-90)
source: ndc

Packages (3)

71205-129-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-30) 71205-129-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-60) 71205-129-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-90)

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": "3bdf016f-4176-4fd8-aae5-c0806d80daee", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897666"], "spl_set_id": ["a6de732a-fe48-486d-bb05-0a9fff6f42d7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-30)", "package_ndc": "71205-129-30", "marketing_start_date": "20181001"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-60)", "package_ndc": "71205-129-60", "marketing_start_date": "20181001"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-129-90)", "package_ndc": "71205-129-90", "marketing_start_date": "20181001"}], "brand_name": "Verapamil Hydrochloride", "product_id": "71205-129_3bdf016f-4176-4fd8-aae5-c0806d80daee", "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": "71205-129", "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": "ANDA070994", "marketing_category": "ANDA", "marketing_start_date": "19861001", "listing_expiration_date": "20261231"}