NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1059Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1059Add 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
72162-1059-27216210590245 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-2)Marketed from May 8, 2023
72162-1059-37216210590330 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-3)Marketed from May 8, 2023
72162-1059-67216210590660 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-6)Marketed from May 8, 2023
72162-1059-97216210590990 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1059-9)Marketed from May 8, 2023

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 Extended ReleaseSuffix: Extended Release
Generic name (nonproprietary)
alprazolam
Active ingredients
Alprazolam — .5 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078056
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 72162-1059_6e4271db-f791-421e-8abd-65feddded931SPL ID 6e4271db-f791-421e-8abd-65feddded931SPL set ID 4f6e4656-689f-46a6-a8ed-54ee55583357RxCUI 433798UNII 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

N472162105902 followed by a unit qualifier and the quantity

Package 72162-1059-02. 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 extended-release tablets are indicated for the treatment of panic disorder with or without agoraphobia, in adults. Alprazolam extended-release tablets are a benzodiazepine indicated for the 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 72162-1059

What is NDC 72162-1059?
72162-1059 is the product NDC for Alprazolam Extended Release (alprazolam), Alprazolam .5 mg/1 tablet, extended release, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Alprazolam Extended Release (Alprazolam).
What is the active ingredient?
Alprazolam.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. 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 Extended Release?
1 other product NDC are listed under this name. See all Alprazolam Extended Release 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 Extended Release NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Alprazolam Extended ReleasealprazolamAlprazolam .5 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-112971335-1129-0171335-1129-0271335-1129-03+2 more

Other NDCs under ANDA 078056

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

FDA NDC Directory listings under ANDA 078056
ProductStrengthForm · routeLabelerProduct NDC
Alprazolam Extended ReleasealprazolamAlprazolam .5 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-1129

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