NDC codes

FDA NDC Directory
Product NDC (as listed)68788-8300Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-8300Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
68788-8300-1687888300011 BOTTLE in 1 CARTON (68788-8300-1) / 118 mL in 1 BOTTLEMarketed from Nov 30, 2022

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
good sense tussin dm
Generic name (nonproprietary)
dextromethorphan hydrobromide, guaifenesin
Active ingredients
Dextromethorphan hydrobromide — 20 mg/20mLGuaifenesin — 200 mg/20mL
Dosage form
Solution
Route
Oral
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 341
Marketing start
Listing expires
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)Sigma-1 Receptor Agonists (Mechanism)Uncompetitive NMDA Receptor Antagonists (Mechanism)
Identifiers
Product ID 68788-8300_9e8df732-dbdb-4d8b-b999-80d910527308SPL ID 9e8df732-dbdb-4d8b-b999-80d910527308SPL set ID 15c8e177-a381-43b2-aed8-d917c7c4372eRxCUI 1790650UNII 9D2RTI9KYH, 495W7451VQ
Pharmacologic class
Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468788830001 followed by a unit qualifier and the quantity

Package 68788-8300-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under 341

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under 341
ProductStrengthForm · routeLabelerProduct NDC
Good Neighbor Pharmacy Childrens Allergydiphenhydramine hydrochlorideDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-7994
Diphenhydramine HClDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-8274
rugby cough syrupdextromethorphan hydrobromide, guaifenesinDextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 200 mg/20mLSolutionOralPreferred Pharmaceuticals Inc68788-8303
Good Sense Childrens Cold and Coughbrompheniramine maleate, dextromethorphan hbr, phenylephrine hclBrompheniramine maleate 2 mg/10mL + 2 more ingredientsSolutionOralPreferred Pharmaceuticals Inc.68788-8331
Diphenhydramine HCLDiphenhydramine hydrochloride 50 mg/1CapsuleOralPreferred Pharmaceuticals, Inc.68788-9688
Diphenhydramine HCLDiphenhydramine hydrochloride 25 mg/1CapsuleOralPreferred Pharmaceuticals, Inc.68788-9687
Banophendiphenhydramine hclDiphenhydramine hydrochloride 50 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-7830

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