Amlodipine,valsartan And Hydrochlorothiazide Tablet, Film Coated
NDC Package 33342-285-10
Package Information
Amlodipine, Valsartan And Hydrochlorothiazide tablets are indicated for the treatment of hypertension, to lower blood pressure. This formulation utilizes a tablet, film coated delivery system. Marketed by Macleods Pharmaceuticals Limited, this product is identified by NDC 33342-285 and is authorized under FDA application ANDA207299.
Identification & Billing
- RxCUI: 848131 - amLODIPine 10 MG / valsartan 160 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
- RxCUI: 848131 - amlodipine 10 MG / hydrochlorothiazide 12.5 MG / valsartan 160 MG Oral Tablet
- RxCUI: 848131 - amlodipine (as amlodipine besylate) 10 MG / HCTZ 12.5 MG / valsartan 160 MG Oral Tablet
- RxCUI: 848131 - amlodipine 10 MG / HCTZ 12.5 MG / valsartan 160 MG Oral Tablet
- RxCUI: 848135 - amLODIPine 10 MG / valsartan 320 MG / hydroCHLOROthiazide 25 MG Oral Tablet
Clinical Specifications
- Angiotensin 2 Receptor Antagonists - [MoA] (Mechanism of Action)
- Angiotensin 2 Receptor Blocker - [EPC] (Established Pharmacologic Class)
- Calcium Channel Antagonists - [MoA] (Mechanism of Action)
- Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
- Cytochrome P450 3A Inhibitors - [MoA] (Mechanism of Action)
- Dihydropyridine Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
- Dihydropyridines - [CS]
- Increased Diuresis - [PE] (Physiologic Effect)
- Thiazide Diuretic - [EPC] (Established Pharmacologic Class)
- Thiazides - [CS]
Regulatory & Marketing
Hierarchy Structure
- 33342 - Macleods Pharmaceuticals Limited
- 33342-285 - Amlodipine, Valsartan And Hydrochlorothiazide
- 33342-285-10 - 90 TABLET, FILM COATED in 1 BOTTLE
- 33342-285 - Amlodipine, Valsartan And Hydrochlorothiazide
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.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (33342-285). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 33342-285-10 identifies a specific commercial package of 90 tablet, film coated in 1 bottle of Amlodipine, Valsartan And Hydrochlorothiazide, a human prescription drug labeled by Macleods Pharmaceuticals Limited. This tablet, film coated is formulated for oral use and contains amlodipine besylate; hydrochlorothiazide; valsartan 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 Macleods Pharmaceuticals Limited on January 06, 2025. The current certification is valid through December 31, 2026.
How is this Macleods Pharmaceuticals Limited product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 33342028510. 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.