Verapamil Hydrochloride Tablet
NDC Package 42291-855-01
Package Information
Verapamil Hydrochloride tablets is uSP are indicated for the treatment of the following:Angina 1.Angina at rest including: -Vasospastic (Prinzmetal's variant) angina -Unstable (crescendo, pre-infarction) angina 2.Chronic stable angina (classic effort-associated angina)Arrhythmias 1.In association with digitalis for the control of ventricular rate at rest and during stress in patients with chronic atrial flutter and/or atrial fibrillation (see WARNINGS: Accessory bypass tract ) 2.Prophylaxis of repetitive paroxysmal supraventricular tachycardiaEssential hypertension Verapamil hydrochloride is indicated for the treatment of hypertension, to lower blood pressure. This formulation utilizes a tablet delivery system. Marketed by Avkare, this product is identified by NDC 42291-855 and is authorized under FDA application ANDA071881.
Identification & Billing
- RxCUI: 897666 - verapamil HCl 120 MG Oral Tablet
- RxCUI: 897666 - verapamil hydrochloride 120 MG Oral Tablet
- RxCUI: 897683 - verapamil HCl 80 MG Oral Tablet
- RxCUI: 897683 - verapamil hydrochloride 80 MG Oral Tablet
- RxCUI: 897722 - verapamil HCl 40 MG 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
- 42291 - Avkare
- 42291-855 - Verapamil Hydrochloride
- 42291-855-01 - 100 TABLET in 1 BOTTLE
- 42291-855 - 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 42291-855-01 identifies a specific commercial package of 100 tablet in 1 bottle of Verapamil Hydrochloride, a human prescription drug labeled by Avkare. This product is billed for "EA" each discreet unit and contains an estimated amount of 100 billable units per package. This tablet 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 Avkare on April 13, 2020. The current certification is valid through December 31, 2027.
How is this Avkare product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 42291085501. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 100 total billable units per package. 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 Product segment to maintain the 5-4-2 structure.