NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4499Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4499Add 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
68071-4499-36807144990330 TABLET, FILM COATED in 1 BOTTLE (68071-4499-3)Marketed from Jul 18, 2018

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)
Hydroxyzine Hydrochloride
Generic name (nonproprietary)
hydroxyzine hydrochloride
Active ingredients
Hydroxyzine dihydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 088617
Marketing start
Listing expires
Other FDA classes
Histamine Receptor Antagonists (Mechanism)
Identifiers
Product ID 68071-4499_1a8d9b76-64fd-adfb-e063-6394a90aafa0SPL ID 1a8d9b76-64fd-adfb-e063-6394a90aafa0SPL set ID 714a26a1-371f-ef23-e053-2a95a90a6af6RxCUI 995218UNII 76755771U3UPC 0368071449938
Pharmacologic class
Antihistamine

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

N468071449903 followed by a unit qualifier and the quantity

Package 68071-4499-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 088617

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

FDA NDC Directory listings under ANDA 088617
ProductStrengthForm · routeLabelerProduct NDC
Hydroxyzine HydrochlorideHydroxyzine dihydrochloride 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-271
Hydroxyzine HydrochlorideHydroxyzine dihydrochloride 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0961
Hydroxyzine HydrochlorideHydroxyzine hydrochloride 10 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-664
Hydroxyzine HydrochlorideHydroxyzine hydrochloride 10 mg/1Tablet, Film coatedOralSt Mary's Medical Park Pharmacy60760-285
Hydroxyzine HydrochlorideHydroxyzine dihydrochloride 10 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-5060
Hydroxyzine HydrochlorideHydroxyzine dihydrochloride 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8738
Hydroxyzine HydrochlorideHydroxyzine dihydrochloride 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4117

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