NDC codes

FDA NDC Directory
Product NDC (as listed)72189-450Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0450Add 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
72189-450-607218904506060 TABLET in 1 BOTTLE (72189-450-60)Marketed from Mar 22, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
Direct_Rx
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203346
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 72189-450_2c4dbbad-3ed5-fec3-e063-6394a90a3b4dSPL ID 2c4dbbad-3ed5-fec3-e063-6394a90a3b4dSPL set ID f77cfdd0-847d-4edd-e053-6394a90a91b7RxCUI 197322UNII 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

N472189045060 followed by a unit qualifier and the quantity

Package 72189-0450-60. 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 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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203346

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

FDA NDC Directory listings under ANDA 203346
ProductStrengthForm · routeLabelerProduct NDC
AlprazolamAlprazolam 1 mg/1TabletOralCoupler LLC67046-0007
AlprazolamAlprazolam 1 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2966
AlprazolamAlprazolam 2 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2976
AlprazolamAlprazolam .25 mg/1TabletOralAurobindo Pharma Limited65862-676
AlprazolamAlprazolam .5 mg/1TabletOralCoupler LLC67046-0154
AlprazolamAlprazolam 1 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0444
AlprazolamAlprazolam .5 mg/1TabletOralAurobindo Pharma Limited65862-677
AlprazolamAlprazolam 1 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-678
AlprazolamAlprazolam 1 mg/1TabletOralAurobindo Pharma Limited65862-678
AlprazolamAlprazolam 2 mg/1TabletOralAurobindo Pharma Limited65862-679
AlprazolamAlprazolam .5 mg/1TabletOralMedsource Pharmaceuticals45865-257
Alprazolam C-IVAlprazolam 1 mg/1TabletOralDirect_Rx72189-443
Alprazolam C-IVAlprazolam .5 mg/1TabletOralDirect_Rx72189-442
AlprazolamAlprazolam .5 mg/1TabletOralAvPAK50268-034
AlprazolamAlprazolam .25 mg/1TabletOralAvPAK50268-033
AlprazolamAlprazolam 1 mg/1TabletOralAvPAK50268-035
AlprazolamAlprazolam 2 mg/1TabletOralBryant Ranch Prepack71335-1894
AlprazolamAlprazolam .25 mg/1TabletOralNorthwind Health Company, LLC82868-061
AlprazolamAlprazolam 1 mg/1TabletOralClinical Solutions Wholesale, LLC58118-0678
AlprazolamAlprazolam .25 mg/1TabletOralClinical Solutions Wholesale, LLC58118-0676

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