NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2447Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2447Add 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
72162-2447-3721622447037216224470330 CAPSULE in 1 BOTTLE (72162-2447-3)Marketed from Nov 14, 2024
72162-2447-9721622447097216224470990 CAPSULE in 1 BOTTLE (72162-2447-9)Marketed from Nov 14, 2024

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)
Silodosin
Generic name (nonproprietary)
silodosin
Active ingredients
Silodosin — 8 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213230
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)
Identifiers
Product ID 72162-2447_5b6204b7-40c1-4071-82f4-ff5fa34c2425SPL ID 5b6204b7-40c1-4071-82f4-ff5fa34c2425SPL set ID aac3314b-af8c-400e-ba91-0cf2b95e70ddRxCUI 809477UNII CUZ39LUY82
Pharmacologic class
alpha-Adrenergic Blocker

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

N472162244703 followed by a unit qualifier and the quantity

Package 72162-2447-03. 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 .

Indications (excerpt from the label)

Silodosin, a selective alpha‑1 adrenergic receptor antagonist, is indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH) [see CLINICAL STUDIES (14) ] . Silodosin capsules is not indicated for the treatment of hypertension. Silodosin capsules, an alpha‑1 adrenergic receptor antagonist, is indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH). Silodosin capsules are not indicated for the treatment of hypertension. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2447

What is NDC 72162-2447?
72162-2447 is the product NDC for Silodosin, Silodosin 8 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Silodosin.
What is the active ingredient?
Silodosin.
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 Silodosin?
28 other product NDCs are listed under this name. See all Silodosin 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 Silodosin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
SilodosinSilodosin 4 mg/1CapsuleOralBryant Ranch Prepack72162-244672162-2446-03
SilodosinSilodosin 4 mg/1CapsuleOralCreekwood Pharmaceuticals LLC82619-11382619-0113-01
SilodosinSilodosin 8 mg/1CapsuleOralCreekwood Pharmaceuticals LLC82619-11482619-0114-0182619-0114-02
SilodosinSilodosin 4 mg/1CapsuleOralAvKARE42291-77742291-0777-30
SilodosinSilodosin 8 mg/1CapsuleOralAvKARE42291-77842291-0778-90
SilodosinSilodosin 4 mg/1CapsuleOralCamber Pharmaceuticals, Inc.31722-63531722-0635-3031722-0635-3131722-0635-90+1 more
SilodosinSilodosin 8 mg/1CapsuleOralCamber Pharmaceuticals, Inc.31722-63631722-0636-3031722-0636-3131722-0636-90+1 more
SilodosinSilodosin 4 mg/1CapsuleOralAlembic Pharmaceuticals Limited46708-40546708-0405-3046708-0405-9046708-0405-91
SilodosinSilodosin 8 mg/1CapsuleOralAlembic Pharmaceuticals Limited46708-40646708-0406-3046708-0406-9046708-0406-91
SilodosinSilodosin 4 mg/1CapsuleOralAlembic Pharmaceuticals Inc.62332-40562332-0405-3062332-0405-9062332-0405-91

All 29 Silodosin NDCs

Other NDCs under ANDA 213230

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

FDA NDC Directory listings under ANDA 213230
ProductStrengthForm · routeLabelerProduct NDC
SilodosinSilodosin 4 mg/1CapsuleOralBryant Ranch Prepack72162-2446
SilodosinSilodosin 4 mg/1CapsuleOralCreekwood Pharmaceuticals LLC82619-113
SilodosinSilodosin 8 mg/1CapsuleOralCreekwood Pharmaceuticals LLC82619-114

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