NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5078Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5078Add 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
50090-5078-05009050780030 TABLET in 1 BOTTLE (50090-5078-0)Marketed from Jun 17, 2020
50090-5078-25009050780260 TABLET in 1 BOTTLE (50090-5078-2)Marketed from Sep 18, 2023
50090-5078-35009050780390 TABLET in 1 BOTTLE (50090-5078-3)Marketed from Jun 17, 2020

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 — .5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074342
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 50090-5078_f8c1781d-12d5-43a2-a215-01ceced386d6SPL ID f8c1781d-12d5-43a2-a215-01ceced386d6SPL set ID 8ef75d22-4a7c-48d5-a532-5a43b8593e7cRxCUI 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

N450090507800 followed by a unit qualifier and the quantity

Package 50090-5078-00. 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. 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)

Other NDCs under ANDA 074342

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

FDA NDC Directory listings under ANDA 074342
ProductStrengthForm · routeLabelerProduct NDC
AlprazolamAlprazolam .5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-313
AlprazolamAlprazolam .5 mg/1TabletOralActavis Pharma, Inc.0228-2029
AlprazolamAlprazolam 1 mg/1TabletOralActavis Pharma, Inc.0228-2031
AlprazolamAlprazolam 2 mg/1TabletOralActavis Pharma, Inc.0228-2039
AlprazolamAlprazolam 1 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-328
AlprazolamAlprazolam .25 mg/1TabletOralBryant Ranch Prepack71335-2133
AlprazolamAlprazolam .25 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-112
AlprazolamAlprazolam 1 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-113
AlprazolamAlprazolam .25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2292
AlprazolamAlprazolam .5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2220
AlprazolamAlprazolam .5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0099
AlprazolamAlprazolam 1 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0110
AlprazolamAlprazolam .5 mg/1TabletOralBryant Ranch Prepack71335-0849
AlprazolamAlprazolam .25 mg/1TabletOralActavis Pharma, Inc.0228-2027

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