Amlodipine And Atorvastatin Tablet, Film Coated
NDC Package 62332-765-30
Package Information
Amlodipine And Atorvastatin tablets are indicated in patients for whom treatment with both amlodipine and atorvastatin is appropriate.AmlodipineHypertension Amlodipine is indicated for the treatment of hypertension, to lower blood pressure. This formulation utilizes a tablet, film coated delivery system. Marketed by Alembic Pharmaceuticals Inc., this product is identified by NDC 62332-765 and is authorized under FDA application ANDA217279.
Identification & Billing
- RxCUI: 404011 - amLODIPine besylate 5 MG / atorvastatin calcium 80 MG Oral Tablet
- RxCUI: 404011 - amlodipine 5 MG / atorvastatin 80 MG Oral Tablet
- RxCUI: 404011 - amlodipine (as amlodipine besylate) 5 MG / atorvastatin (as atorvastatin calcium) 80 MG Oral Tablet
- RxCUI: 404013 - amLODIPine besylate 10 MG / atorvastatin calcium 80 MG Oral Tablet
- RxCUI: 404013 - amlodipine 10 MG / atorvastatin 80 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)
- Dihydropyridine Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
- Dihydropyridines - [CS]
- HMG-CoA Reductase Inhibitor - [EPC] (Established Pharmacologic Class)
- Hydroxymethylglutaryl-CoA Reductase Inhibitors - [MoA] (Mechanism of Action)
Regulatory & Marketing
Hierarchy Structure
- 62332 - Alembic Pharmaceuticals Inc.
- 62332-765 - Amlodipine And Atorvastatin
- 62332-765-30 - 30 TABLET, FILM COATED in 1 BOTTLE
- 62332-765 - Amlodipine And Atorvastatin
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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Other Available Packages
The following commercial packages are registered under the same Product NDC (62332-765). 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 62332-765-30 identifies a specific commercial package of 30 tablet, film coated in 1 bottle of Amlodipine And Atorvastatin, a human prescription drug labeled by Alembic Pharmaceuticals Inc.. This tablet, film coated is formulated for oral use and contains amlodipine besylate; atorvastatin calcium trihydrate 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 Alembic Pharmaceuticals Inc. on May 23, 2025. The current certification is valid through December 31, 2026.
How is this Alembic Pharmaceuticals Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 62332076530. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 30 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.