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
68788-7830-1687887830016878878300115 CAPSULE in 1 BOTTLE (68788-7830-1)Marketed from Jan 8, 2021
68788-7830-3687887830036878878300330 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
Labeler
Preferred Pharmaceuticals Inc.NDC labeler code 68788
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)

About NDC 68788-7830

What is NDC 68788-7830?
68788-7830 is the product NDC for Banophen (diphenhydramine hcl), Diphenhydramine hydrochloride 50 mg/1 capsule, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Banophen (Diphenhydramine hcl).
What is the active ingredient?
Diphenhydramine hydrochloride.
Who is the labeler?
Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Banophen?
8 other product NDCs are listed under this name. See all Banophen NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Banophen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Banophendiphenhydramine hclDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralHealth Department, Oklahoma State83112-55583112-0555-59
Banophendiphenhydramine hclDiphenhydramine hydrochloride 50 mg/1CapsuleOralMajor Pharmaceuticals0904-530700904-5307-6000904-5307-80
Banophendiphenhydramine hclDiphenhydramine hydrochloride 50 mg/1CapsuleOralBryant Ranch Prepack63629-945163629-9451-0163629-9451-02
Banophendiphenhydramine hclDiphenhydramine hydrochloride 50 mg/1CapsuleOralBryant Ranch Prepack71335-008171335-0081-0071335-0081-0171335-0081-02+7 more
Banophendiphenhydramine hydrochloride, zinc acetateDiphenhydramine hydrochloride 2 g/100g; Zinc acetate .1 g/100gCreamTopicalMajor Pharmaceuticals0904-535400904-5354-31
Banophendiphenhydramine hclDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-555100904-5551-2400904-5551-59
Banophendiphenhydramine hclDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-554650090-5546-00
Banophendiphenhydramine hclDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralProficient Rx LP71205-61171205-0611-2071205-0611-3071205-0611-60+1 more

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
Diphenhydramine HClDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-8274
Diphenhydramine HCLDiphenhydramine hydrochloride 25 mg/1CapsuleOralPreferred Pharmaceuticals, Inc.68788-9687
Diphenhydramine HCLDiphenhydramine hydrochloride 50 mg/1CapsuleOralPreferred Pharmaceuticals, Inc.68788-9688
Good Neighbor Pharmacy Childrens Allergydiphenhydramine hydrochlorideDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-7994
Good Sense Childrens Cold and Coughbrompheniramine maleate, dextromethorphan hbr, phenylephrine hclBrompheniramine maleate 2 mg/10mL + 2 more ingredientsSolutionOralPreferred Pharmaceuticals Inc.68788-8331
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

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