verapamil hydrochloride
Generic: verapamil hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
verapamil hydrochloride
Generic Name
verapamil hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
verapamil hydrochloride 120 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8338
Product ID
68788-8338_c68a7572-2ab6-427e-87a1-a10cbe6c719d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071881
Listing Expiration
2026-12-31
Marketing Start
2023-02-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888338
Hyphenated Format
68788-8338
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
ANDA071881 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 120 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (68788-8338-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c68a7572-2ab6-427e-87a1-a10cbe6c719d", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897666"], "spl_set_id": ["c7a54ee0-80c0-4c7e-a6a3-cb60142f860c"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8338-3)", "package_ndc": "68788-8338-3", "marketing_start_date": "20230202"}], "brand_name": "VERAPAMIL HYDROCHLORIDE", "product_id": "68788-8338_c68a7572-2ab6-427e-87a1-a10cbe6c719d", "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": "68788-8338", "generic_name": "VERAPAMIL HYDROCHLORIDE", "labeler_name": "Preferred 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": "20230202", "listing_expiration_date": "20261231"}