verapamil hydrochloride
Generic: verapamil hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
verapamil hydrochloride
Generic Name
verapamil hydrochloride
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
verapamil hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4513
Product ID
70518-4513_42b0dc89-b6da-5a4b-e063-6394a90a56e4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206173
Listing Expiration
2026-12-31
Marketing Start
2025-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184513
Hyphenated Format
70518-4513
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-4513-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42b0dc89-b6da-5a4b-e063-6394a90a56e4", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897640"], "spl_set_id": ["d7c29dfd-3968-41ac-a081-e670f9bd605c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4513-0)", "package_ndc": "70518-4513-0", "marketing_start_date": "20251101"}], "brand_name": "VERAPAMIL HYDROCHLORIDE", "product_id": "70518-4513_42b0dc89-b6da-5a4b-e063-6394a90a56e4", "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": "70518-4513", "generic_name": "VERAPAMIL HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VERAPAMIL HYDROCHLORIDE", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA206173", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}