NDC codes

FDA NDC Directory
Product NDC (as listed)60687-377Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0377Add 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
60687-377-0160687037701100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-377-01) / 1 TABLET in 1 BLISTER PACK (60687-377-11)Marketed from Nov 9, 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 — .25 mg/1
Dosage form
Tablet
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
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 60687-377_2a81392c-12be-e4aa-e063-6394a90a3d45SPL ID 2a81392c-12be-e4aa-e063-6394a90a3d45SPL set ID ea95d182-453b-4c43-8402-d65c488d55f2RxCUI 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

N460687037701 followed by a unit qualifier and the quantity

Package 60687-0377-01. 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 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 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 60687-377

What is NDC 60687-377?
60687-377 is the product NDC for Alprazolam, Alprazolam .25 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, 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?
American Health Packaging, NDC labeler code 60687. 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?
120 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/1TabletOralNatco Pharma USA LLC69339-19969339-0199-0169339-0199-0569339-0199-10

All 121 Alprazolam NDCs

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/1TabletOralPreferredPharmaceuticals Inc.68788-8394
AlprazolamAlprazolam 1 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0444
AlprazolamAlprazolam .5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8410
AlprazolamAlprazolam .25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8414
AlprazolamAlprazolam .25 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3817
AlprazolamAlprazolam .5 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3818
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 .5 mg/1TabletOralAurobindo Pharma Limited65862-677
AlprazolamAlprazolam 1 mg/1TabletOralAurobindo Pharma Limited65862-678
AlprazolamAlprazolam 1 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-678
AlprazolamAlprazolam 2 mg/1TabletOralAurobindo Pharma Limited65862-679
AlprazolamAlprazolam .5 mg/1TabletOralMedsource Pharmaceuticals45865-257
AlprazolamAlprazolam .25 mg/1TabletOralNorthwind Health Company, LLC82868-061
Alprazolam C-IVAlprazolam .5 mg/1TabletOralDirect_Rx72189-442
Alprazolam C-IVAlprazolam 1 mg/1TabletOralDirect_Rx72189-443
AlprazolamAlprazolam 2 mg/1TabletOralDirect_Rx72189-450

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