NDC codes

FDA NDC Directory
Product NDC (as listed)59762-0066Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59762-0066Add 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
59762-0066-15976200660160 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0066-1)Marketed from Jan 17, 2003

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)
Alprazolam XRSuffix: XR
Generic name (nonproprietary)
alprazolam
Active ingredients
Alprazolam — 2 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 021434
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 59762-0066_70f0098e-50b5-4e61-b4e0-141a55d92267SPL ID 70f0098e-50b5-4e61-b4e0-141a55d92267SPL set ID 1338d1c9-7c75-42ed-95f3-9eb1b6fc51d3RxCUI 433798, 433799, 433800, 433801UNII YU55MQ3IZY
Pharmacologic class
Benzodiazepine

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

N459762006601 followed by a unit qualifier and the quantity

Package 59762-0066-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Alprazolam XR is indicated for the treatment of panic disorder with or without agoraphobia, in adults. Alprazolam XR is a benzodiazepine indicated for the treatment of panic disorder with or without agoraphobia, in adults. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 021434

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

FDA NDC Directory listings under NDA 021434
ProductStrengthForm · routeLabelerProduct NDC
Alprazolam XRalprazolamAlprazolam 1 mg/1Tablet, Extended releaseOralMylan Pharmaceuticals Inc.59762-0059
Alprazolam XRalprazolamAlprazolam .5 mg/1Tablet, Extended releaseOralMylan Pharmaceuticals Inc.59762-0057
Alprazolam XRalprazolamAlprazolam 3 mg/1Tablet, Extended releaseOralMylan Pharmaceuticals Inc.59762-0068
Xanax XRalprazolamAlprazolam 2 mg/1Tablet, Extended releaseOralViatris Specialty LLC58151-505
Xanax XRalprazolamAlprazolam 3 mg/1Tablet, Extended releaseOralViatris Specialty LLC58151-506

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Alprazolam XR (alprazolam) NDC 59762-0066 | Med-Code