NDC codes

FDA NDC Directory
Product NDC (as listed)59762-3722Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59762-3722Add 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
59762-3722-159762372201100 TABLET in 1 BOTTLE (59762-3722-1)Marketed from Oct 16, 1981
59762-3722-359762372203500 TABLET in 1 BOTTLE (59762-3722-3)Marketed from Oct 16, 1981

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
Generic name (nonproprietary)
alprazolam
Active ingredients
Alprazolam — 2 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Mylan Pharmaceuticals Inc.NDC labeler code 59762
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 018276
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 59762-3722_0deddc26-2764-4879-a0e4-a29fff246244SPL ID 0deddc26-2764-4879-a0e4-a29fff246244SPL set ID 13930c94-d83a-414f-be35-b1fef35f738dRxCUI 197321, 197322, 308047, 308048UNII 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

N459762372201 followed by a unit qualifier and the quantity

Package 59762-3722-01. 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 is indicated for the: • acute treatment of generalized anxiety disorder (GAD) in adults. • treatment of panic disorder (PD), with or without agoraphobia in adults. Alprazolam is a benzodiazepine indicated for the: • Acute treatment of generalized anxiety disorder in adults. ( 1 ) • 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)

About NDC 59762-3722

What is NDC 59762-3722?
59762-3722 is the product NDC for Alprazolam, Alprazolam 2 mg/1 tablet, listed with the FDA by Mylan Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Alprazolam.
What is the active ingredient?
Alprazolam.
Who is the labeler?
Mylan Pharmaceuticals Inc., NDC labeler code 59762. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Alprazolam?
114 other product NDCs are listed under this name. See all Alprazolam 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 Alprazolam NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AlprazolamAlprazolam 1 mg/1TabletOralCoupler LLC67046-000767046-0007-03
AlprazolamAlprazolam .5 mg/1TabletOralCoupler LLC67046-015467046-0154-03
AlprazolamAlprazolam .25 mg/1TabletOralAvPAK50268-03350268-0033-15
AlprazolamAlprazolam .5 mg/1TabletOralAvPAK50268-03450268-0034-15
AlprazolamAlprazolam 1 mg/1TabletOralAvPAK50268-03550268-0035-15
AlprazolamAlprazolam 1 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-044480425-0444-0180425-0444-02
AlprazolamAlprazolam .25 mg/1TabletOralNorthwind Health Company, LLC82868-06182868-0061-30
AlprazolamAlprazolam 1 mg/1TabletOralREMEDYREPACK INC.70518-413770518-4137-00
AlprazolamAlprazolam .5 mg/1TabletOralAmerican Health Packaging60687-38860687-0388-01
AlprazolamAlprazolam .25 mg/1TabletOralAmerican Health Packaging60687-37760687-0377-01

All 115 Alprazolam NDCs

Other NDCs under NDA 018276

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

FDA NDC Directory listings under NDA 018276
ProductStrengthForm · routeLabelerProduct NDC
AlprazolamAlprazolam .25 mg/1TabletOralMylan Pharmaceuticals Inc.59762-3719
AlprazolamAlprazolam .5 mg/1TabletOralMylan Pharmaceuticals Inc.59762-3720
AlprazolamAlprazolam 1 mg/1TabletOralMylan Pharmaceuticals Inc.59762-3721
AlprazolamAlprazolam 2 mg/1TabletOralProficient Rx LP63187-971
AlprazolamAlprazolam 1 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC67544-347
AlprazolamAlprazolam .25 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC67544-414
AlprazolamAlprazolam .5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC67544-415
AlprazolamAlprazolam 1 mg/1TabletOralProficient Rx LP71205-614
AlprazolamAlprazolam .5 mg/1TabletOralProficient Rx LP71205-652
AlprazolamAlprazolam 1 mg/1TabletOralAsclemed USA, Inc.76420-663
AlprazolamAlprazolam .25 mg/1TabletOralAsclemed USA, Inc.76420-664
AlprazolamAlprazolam .5 mg/1TabletOralAsclemed USA, Inc.76420-665
AlprazolamAlprazolam 2 mg/1TabletOralAsclemed USA, Inc.76420-666
AlprazolamAlprazolam .25 mg/1TabletOralProficient Rx LP82804-027
XanaxalprazolamAlprazolam .25 mg/1TabletOralPHARMACIA & UPJOHN COMPANY LLC0009-0029
XanaxalprazolamAlprazolam 1 mg/1TabletOralPHARMACIA & UPJOHN COMPANY LLC0009-0090
XanaxalprazolamAlprazolam 2 mg/1TabletOralPHARMACIA & UPJOHN COMPANY LLC0009-0094
XanaxalprazolamAlprazolam .25 mg/1TabletOralViatris Specialty LLC58151-452
XanaxalprazolamAlprazolam .5 mg/1TabletOralViatris Specialty LLC58151-453
XanaxalprazolamAlprazolam 1 mg/1TabletOralViatris Specialty LLC58151-454

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