What is NDC 0781-1089?

0781-1089 is the product NDC for Alprazolam, Alprazolam 2 mg/1 tablet, listed with the FDA by Sandoz Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

Sandoz Inc, NDC labeler code 0781. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Alprazolam NDC 0781-1089 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0781-1089Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00781-1089Add 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 NDC	11-digit (billing)	Package	Copy
0781-1089-01	00781108901	100 TABLET in 1 BOTTLE (0781-1089-01)Marketed from Mar 25, 1998
0781-1089-05	00781108905	500 TABLET in 1 BOTTLE (0781-1089-05)Marketed from Mar 25, 1998

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): Alprazolam
Generic name (nonproprietary): alprazolam
Active ingredients: Alprazolam — 2 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Sandoz IncNDC labeler code 0781
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074909
Marketing start: Mar 25, 1998
Marketing end: Mar 19, 2027
DEA schedule: CIV
Other FDA classes: Benzodiazepines (Chemical structure)
Identifiers: Product ID 0781-1089_4c8c7366-aa3b-4124-9d64-67fb0ead6e15SPL ID 4c8c7366-aa3b-4124-9d64-67fb0ead6e15SPL set ID d9b0e228-17cf-40d7-b62e-5050311c571cRxCUI 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

N400781108901 followed by a unit qualifier and the quantity

Package 00781-1089-01. 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 May 31, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Alprazolam tablets are indicated for the: • acute treatment of generalized anxiety disorder (GAD) in adults. • treatment of panic disorder (PD), with or without agoraphobia in adults. Alprazolam tablets are 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 0781-1089

What is NDC 0781-1089?: 0781-1089 is the product NDC for Alprazolam, Alprazolam 2 mg/1 tablet, listed with the FDA by Sandoz 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?: Sandoz Inc, NDC labeler code 0781. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Alprazolam	Alprazolam 1 mg/1	TabletOral	Coupler LLC	67046-0007	67046-0007-03
Alprazolam	Alprazolam .5 mg/1	TabletOral	Coupler LLC	67046-0154	67046-0154-03
Alprazolam	Alprazolam .25 mg/1	TabletOral	AvPAK	50268-033	50268-0033-15
Alprazolam	Alprazolam .5 mg/1	TabletOral	AvPAK	50268-034	50268-0034-15
Alprazolam	Alprazolam 1 mg/1	TabletOral	AvPAK	50268-035	50268-0035-15
Alprazolam	Alprazolam 1 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0444	80425-0444-0180425-0444-02
Alprazolam	Alprazolam .25 mg/1	TabletOral	Northwind Health Company, LLC	82868-061	82868-0061-30
Alprazolam	Alprazolam 1 mg/1	TabletOral	REMEDYREPACK INC.	70518-4137	70518-4137-00
Alprazolam	Alprazolam .5 mg/1	TabletOral	American Health Packaging	60687-388	60687-0388-01
Alprazolam	Alprazolam .25 mg/1	TabletOral	American Health Packaging	60687-377	60687-0377-01

All 115 Alprazolam NDCs

Other NDCs under ANDA 074909

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

FDA NDC Directory listings under ANDA 074909
Product	Strength	Form · route	Labeler	Product NDC
Alprazolam	Alprazolam 2 mg/1	TabletOral	A-S Medication Solutions	50090-2819
Alprazolam	Alprazolam 2 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	55289-523
Alprazolam	Alprazolam 2 mg/1	TabletOral	Proficient Rx LP	63187-444
Alprazolam	Alprazolam 2 mg/1	TabletOral	Bryant Ranch Prepack	71335-0920