Maximum Strength Tussin Dm Liquid Filled Softgels Capsule, Liquid Filled
NDC Package 76281-601-02
Package Information
Maximum Strength Tussin Dm Liquid Filled Softgels (dextromethorphan hbr, guaifenesin) capsules is uses• helps loosen phlegm (mucus) and thin bronchial secretions to make cough more productive• temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Aptapharma Inc., this product is identified by NDC 76281-601 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1111663 - dextromethorphan HBr 10 MG / guaiFENesin 200 MG Oral Capsule
- RxCUI: 1111663 - dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG Oral Capsule
Clinical Specifications
- 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)
Regulatory & Marketing
Hierarchy Structure
- 76281 - Aptapharma Inc.
- 76281-601 - Maximum Strength Tussin Dm Liquid Filled Softgels
- 76281-601-02 - 2 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- 76281-601 - Maximum Strength Tussin Dm Liquid Filled Softgels
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 76281-601-02 identifies a specific commercial package of 2 blister pack in 1 carton / 10 capsule, liquid filled in 1 blister pack of Maximum Strength Tussin Dm Liquid Filled Softgels, a human over the counter drug labeled by Aptapharma Inc.. This capsule, liquid filled is formulated for oral use and contains dextromethorphan hydrobromide; guaifenesin 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 Aptapharma Inc. on January 01, 2026. The current certification is valid through December 31, 2027.
How is this Aptapharma Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 76281060102. 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.