NDC codes

FDA NDC Directory
Product NDC (as listed)29300-360Labeler and product segments. Claims need a package NDC.
Product NDC at billing width29300-0360Add 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
29300-360-012930003600129300036001100 TABLET in 1 BOTTLE (29300-360-01)Marketed from Nov 2, 2026
29300-360-052930003600529300036005500 TABLET in 1 BOTTLE (29300-360-05)Marketed from Nov 2, 2026
29300-360-1029300036010293000360101000 TABLET in 1 BOTTLE (29300-360-10)Marketed from Nov 2, 2026

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
Unichem Pharmaceuticals (USA), Inc.NDC labeler code 29300
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213204
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 29300-360_a806e27a-19e4-4780-b622-d9c9a062b37fSPL ID a806e27a-19e4-4780-b622-d9c9a062b37fSPL set ID e42f1683-bc3e-4bef-9305-ddf1aed65f86UNII 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

N429300036001 followed by a unit qualifier and the quantity

Package 29300-0360-01. 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 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 29300-360

What is NDC 29300-360?
29300-360 is the product NDC for Alprazolam, Alprazolam .25 mg/1 tablet, listed with the FDA by Unichem Pharmaceuticals (USA), Inc.. It has 3 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?
Unichem Pharmaceuticals (USA), Inc., NDC labeler code 29300. 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?
124 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 .5 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-36129300-0361-0129300-0361-0529300-0361-10
AlprazolamAlprazolam 1 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-36229300-0362-0129300-0362-0529300-0362-10
AlprazolamAlprazolam 2 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-36329300-0363-0129300-0363-0529300-0363-10
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

All 125 Alprazolam NDCs

Other NDCs under ANDA 213204

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

FDA NDC Directory listings under ANDA 213204
ProductStrengthForm · routeLabelerProduct NDC
AlprazolamAlprazolam .5 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-361
AlprazolamAlprazolam 1 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-362
AlprazolamAlprazolam 2 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-363

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