NDC codes

FDA NDC Directory
Product NDC (as listed)68788-7830Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-7830Add 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
68788-7830-16878878300115 CAPSULE in 1 BOTTLE (68788-7830-1)Marketed from Jan 8, 2021
68788-7830-36878878300330 CAPSULE in 1 BOTTLE (68788-7830-3)Marketed from Jan 8, 2021

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)
Banophen
Generic name (nonproprietary)
diphenhydramine hcl
Active ingredients
Diphenhydramine hydrochloride — 50 mg/1
Dosage form
Capsule
Route
Oral
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 341
Marketing start
Marketing end
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68788-7830_241c4be4-79e6-41e5-a2b3-2cd460d51088SPL ID 241c4be4-79e6-41e5-a2b3-2cd460d51088SPL set ID 0f52270a-b11a-4fa1-aac2-9fe5ff625419RxCUI 1020477, 1020479UNII TC2D6JAD40
Pharmacologic class
Histamine-1 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

N468788783001 followed by a unit qualifier and the quantity

Package 68788-7830-01. 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)

Use Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies • runny nose • sneezing • itchy, watery eyes • itchy throat and nose • Temporarily relieves these symptoms due to the common cold o runny nose o sneezing

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
good sense tussin dmdextromethorphan hydrobromide, guaifenesinDextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 200 mg/20mLSolutionOralPreferred Pharmaceuticals Inc.68788-8300
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

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