Dexamethasone Tablet
NDC Package 68047-702-01
Package Information
Dexamethasone (dexamethasone 1.5 mg) tablets is dexamethasone is used to treat conditions such as arthritis, blood/hormone disorders, allergic reactions, skin diseases, eye problems, breathing problems, bowel disorders, cancer, and immune system disorders. This formulation utilizes a tablet delivery system. Marketed by Larken Laboratories, Inc., this product is identified by NDC 68047-702 and is authorized under FDA application ANDA201270.
Identification & Billing
- RxCUI: 197580 - dexAMETHasone 1.5 MG Oral Tablet
- RxCUI: 197580 - dexamethasone 1.5 MG Oral Tablet
- RxCUI: 759481 - {51 (dexamethasone 1.5 MG Oral Tablet) } Pack
- RxCUI: 759481 - dexAMETHasone 1.5 MG Tablet 13 Day 51 Count Pack
- RxCUI: 759697 - {35 (dexamethasone 1.5 MG Oral Tablet) } Pack
Clinical Specifications
- Oral - Administration to or by way of the mouth.
- Oral - Administration to or by way of the mouth.
Regulatory & Marketing
Hierarchy Structure
- 68047 - Larken Laboratories, Inc.
- 68047-702 - Dexamethasone
- 68047-702-01 - 100 TABLET in 1 BOTTLE
- 68047-702 - Dexamethasone
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 (68047-702). 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 68047-702-01 identifies a specific commercial package of 100 tablet in 1 bottle of Dexamethasone 1.5 Mg, a human prescription drug labeled by Larken Laboratories, Inc.. This tablet is formulated for oral use and contains dexamethasone 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 Larken Laboratories, Inc. on September 01, 2017. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Dexamethasone is used to treat conditions such as arthritis, blood/hormone disorders, allergic reactions, skin diseases, eye problems, breathing problems, bowel disorders, cancer, and immune system disorders. It is also used as a test for an adrenal gland disorder (Cushing's syndrome). Dexamethasone belongs to a class of drugs known as corticosteroids. It decreases your immune system's response to various diseases to reduce symptoms such as swelling and allergic-type reactions.
How is this Larken Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 68047070201. 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.