Aquasol A Injection, Solution
NDC Package 70199-026-11
Package Information
Aquasol A (vitamin a palmitate) injection is vitamin A injection is effective for the treatment of vitamin A deficiency.The parenteral administration is indicated when the oral administration is not feasible as in anorexia, nausea, vomiting, pre- and postoperative conditions, or it is not available as in the "Malabsorption Syndrome" with accompanying steatorrhea.Pediatric Use: Vitamin A treatment for deficiency states has been recognized as an especially effective and important therapy in the pediatric population.Vitamin A supplementation for deficiency states in this population has been addressed by the Committee on Clinical Practice Issues of the American Society for Clinical Nutrition, by the American Society for Parenteral and Enteral Nutrition, and by the World Health Organization. This formulation utilizes a injection, solution delivery system. Marketed by Casper Pharma Llc, this product is identified by NDC 70199-026 and is authorized under FDA application NDA006823.
Identification & Billing
- RxCUI: 210972 - Aquasol A 50,000 UNT/ML in 2 ML Injection
- RxCUI: 210972 - 2 ML vitamin A 50000 UNT/ML Injection [Aquasol A]
- RxCUI: 210972 - Aquasol A 50,000 UNT/ML (as retinol 15 MG/ML) per 2 ML Injection
- RxCUI: 210972 - Aquasol A 50,000 UNT/ML per 2 ML Injection
- RxCUI: 313650 - vitamin A 50,000 UNT/ML in 2 ML Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 70199 - Casper Pharma Llc
- 70199-026 - Aquasol A
- 70199-026-11 - 1 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE
- 70199-026 - Aquasol A
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 70199-026-11 identifies a specific commercial package of 1 vial, single-dose in 1 carton / 2 ml in 1 vial, single-dose of Aquasol A, a human prescription drug labeled by Casper Pharma Llc. This injection, solution is formulated for intramuscular use and contains vitamin a palmitate 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 Casper Pharma Llc on October 01, 2020. The current certification is valid through December 31, 2026.
How is this Casper Pharma Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 70199002611. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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.