verapamil hydrochloride
Generic: verapamil hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
verapamil hydrochloride
Generic Name
verapamil hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
verapamil hydrochloride 240 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55289-723
Product ID
55289-723_47e39c2d-9144-24b3-e063-6294a90a04d4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078906
Listing Expiration
2027-12-31
Marketing Start
2009-09-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55289723
Hyphenated Format
55289-723
Supplemental Identifiers
RxCUI
UPC
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
ANDA078906 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 240 mg/1
Packaging
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-723-30)
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-723-90)
- 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-723-93)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e39c2d-9144-24b3-e063-6294a90a04d4", "openfda": {"upc": ["0355289723301"], "unii": ["V3888OEY5R"], "rxcui": ["897649"], "spl_set_id": ["3c215e6c-d85a-4102-a1c2-f00fa3169a55"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-723-30)", "package_ndc": "55289-723-30", "marketing_start_date": "20151102"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-723-90)", "package_ndc": "55289-723-90", "marketing_start_date": "20151102"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-723-93)", "package_ndc": "55289-723-93", "marketing_start_date": "20151102"}], "brand_name": "verapamil hydrochloride", "product_id": "55289-723_47e39c2d-9144-24b3-e063-6294a90a04d4", "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": "55289-723", "generic_name": "verapamil hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "verapamil hydrochloride", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "ANDA078906", "marketing_category": "ANDA", "marketing_start_date": "20090917", "listing_expiration_date": "20271231"}