NDC codes

FDA NDC Directory
Product NDC (as listed)0009-0094Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00009-0094Add 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
0009-0094-010000900940100009009401100 TABLET in 1 BOTTLE (0009-0094-01)Marketed from Oct 16, 1981

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Xanax
Generic name (nonproprietary)
alprazolam
Active ingredients
Alprazolam — 2 mg/1
Dosage form
Tablet
Route
Oral
Labeler
PHARMACIA & UPJOHN COMPANY LLCNDC labeler code 0009
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 018276
Marketing start
Marketing end
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 0009-0094_f5323eac-81d0-4096-ac15-2f25220c5c28SPL ID f5323eac-81d0-4096-ac15-2f25220c5c28SPL set ID 388e249d-b9b6-44c3-9f8f-880eced0239fRxCUI 141927, 141928, 197321, 197322, 214003, 214004, 308047, 308048UNII YU55MQ3IZYUPC 0300090094010, 0300090090012, 0300090029012, 0300090055011
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

N400009009401 followed by a unit qualifier and the quantity

Package 00009-0094-01. 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)

XANAX is indicated for the: • acute treatment of generalized anxiety disorder (GAD) in adults. • treatment of panic disorder (PD), with or without agoraphobia in adults. XANAX 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 0009-0094

What is NDC 0009-0094?
0009-0094 is the product NDC for Xanax (alprazolam), Alprazolam 2 mg/1 tablet, listed with the FDA by PHARMACIA & UPJOHN COMPANY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Xanax (Alprazolam).
What is the active ingredient?
Alprazolam.
Who is the labeler?
PHARMACIA & UPJOHN COMPANY LLC, NDC labeler code 0009. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Xanax?
6 other product NDCs are listed under this name. See all Xanax 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 Xanax NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
XanaxalprazolamAlprazolam .25 mg/1TabletOralViatris Specialty LLC58151-45258151-0452-0158151-0452-05
XanaxalprazolamAlprazolam 2 mg/1TabletOralViatris Specialty LLC58151-45558151-0455-01
XanaxalprazolamAlprazolam 1 mg/1TabletOralViatris Specialty LLC58151-45458151-0454-0158151-0454-05
XanaxalprazolamAlprazolam .5 mg/1TabletOralViatris Specialty LLC58151-45358151-0453-0158151-0453-05
XanaxalprazolamAlprazolam .25 mg/1TabletOralPHARMACIA & UPJOHN COMPANY LLC0009-002900009-0029-0100009-0029-02
XanaxalprazolamAlprazolam 1 mg/1TabletOralPHARMACIA & UPJOHN COMPANY LLC0009-009000009-0090-04

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/1TabletOralMylan Pharmaceuticals Inc.59762-3722
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 .25 mg/1TabletOralViatris Specialty LLC58151-452
XanaxalprazolamAlprazolam .5 mg/1TabletOralViatris Specialty LLC58151-453
XanaxalprazolamAlprazolam 1 mg/1TabletOralViatris Specialty LLC58151-454

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