Aquanaz Tablet
NDC Package 29978-587-01
Package Information
Aquanaz (dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride) tablets is adults and children 12 years and older: Take 1tablet every 4-6 hours as needed, do not exceed 4 tablets in 24hours, or as directed by a doctor.Children 6-12 years: Take ½ tablet every 4-6 hours as needed, do not exceed 2 tablets in 24 hours, or as directed by a doctor. This formulation utilizes a tablet delivery system. Marketed by Capital Pharmaceutical, Llc, this product is identified by NDC 29978-587.
Identification & Billing
- RxCUI: 1552200 - dextromethorphan HBr 15 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG Oral Tablet
- RxCUI: 1552200 - dextromethorphan hydrobromide 15 MG / guaifenesin 400 MG / phenylephrine hydrochloride 10 MG Oral Tablet
Clinical Specifications
- Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
- Decreased Respiratory Secretion Viscosity - [PE] (Physiologic Effect)
- Expectorant - [EPC] (Established Pharmacologic Class)
- Increased Respiratory Secretions - [PE] (Physiologic Effect)
- Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
- Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
- Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
- Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
- alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 29978 - Capital Pharmaceutical, Llc
- 29978-587 - Aquanaz
- 29978-587-01 - 100 TABLET in 1 BOTTLE
- 29978-587 - Aquanaz
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 29978-587-01 identifies a specific commercial package of 100 tablet in 1 bottle of Aquanaz, a human over the counter drug labeled by Capital Pharmaceutical, Llc. 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 dextromethorphan hydrobromide; guaifenesin; phenylephrine 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 Capital Pharmaceutical, Llc on March 10, 2015. The current certification is valid through December 31, 2026.
How is this Capital Pharmaceutical, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 29978058701. 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.