Verapamil Hydrochloride Tablet, Film Coated, Extended Release
NDC Package 68071-3446-0
Package Information
Verapamil Hydrochloride tablets is verapamil hydrochloride extended-release tablets are indicated for the treatment of hypertension, to lower blood pressure. This formulation utilizes a tablet, film coated, extended release delivery system. Marketed by Nucare Pharmaceuticals,inc., this product is identified by NDC 68071-3446 and is authorized under FDA application ANDA090700.
Identification & Billing
- RxCUI: 897659 - verapamil HCl 120 MG Extended Release Oral Tablet
- RxCUI: 897659 - verapamil hydrochloride 120 MG Extended Release Oral Tablet
Clinical Specifications
- Calcium Channel Antagonists - [MoA] (Mechanism of Action)
- Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
- Cytochrome P450 3A Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 3A4 Inhibitors - [MoA] (Mechanism of Action)
- P-Glycoprotein Inhibitors - [MoA] (Mechanism of Action)
Regulatory & Marketing
Hierarchy Structure
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-3446 - Verapamil Hydrochloride
- 68071-3446-0 - 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
- 68071-3446 - Verapamil Hydrochloride
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 68071-3446-0 identifies a specific commercial package of 100 tablet, film coated, extended release in 1 bottle of Verapamil Hydrochloride, a human prescription drug labeled by Nucare Pharmaceuticals,inc.. This tablet, film coated, extended release is formulated for oral use and contains verapamil hydrochloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Nucare Pharmaceuticals,inc. on August 05, 2011. The current certification is valid through December 31, 2026.
How is this Nucare Pharmaceuticals,inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 68071344600. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.