What is NDC 71335-3128?

71335-3128 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.

Bryant Ranch Prepack, NDC labeler code 71335. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Silodosin NDC 71335-3128 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-3128Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-3128Add 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 NDC	11-digit (billing)	Package	Copy
71335-3128-1	7133531280171335312801	30 CAPSULE in 1 BOTTLE (71335-3128-1)Marketed from Apr 29, 2026
71335-3128-2	7133531280271335312802	90 CAPSULE in 1 BOTTLE (71335-3128-2)Marketed from Apr 29, 2026

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 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211166
Marketing start: Dec 3, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 71335-3128_88136a96-4e67-477f-8f35-d2b2f99cce08SPL ID 88136a96-4e67-477f-8f35-d2b2f99cce08SPL set ID afbf4823-8663-4152-9346-ca42c7b7d722RxCUI 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

N471335312801 followed by a unit qualifier and the quantity

Package 71335-3128-01. 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 Jul 7, 2026.

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 is not indicated for the treatment of hypertension. Silodosin, an alpha-1 adrenergic receptor antagonist, is indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH). Silodosin is 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 71335-3128

What is NDC 71335-3128?: 71335-3128 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 71335. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Silodosin	Silodosin 4 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-2446	72162-2446-03
Silodosin	Silodosin 8 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-2447	72162-2447-0372162-2447-09
Silodosin	Silodosin 4 mg/1	CapsuleOral	Creekwood Pharmaceuticals LLC	82619-113	82619-0113-01
Silodosin	Silodosin 8 mg/1	CapsuleOral	Creekwood Pharmaceuticals LLC	82619-114	82619-0114-0182619-0114-02
Silodosin	Silodosin 4 mg/1	CapsuleOral	AvKARE	42291-777	42291-0777-30
Silodosin	Silodosin 8 mg/1	CapsuleOral	AvKARE	42291-778	42291-0778-90
Silodosin	Silodosin 4 mg/1	CapsuleOral	Camber Pharmaceuticals, Inc.	31722-635	31722-0635-3031722-0635-3131722-0635-90+1 more
Silodosin	Silodosin 8 mg/1	CapsuleOral	Camber Pharmaceuticals, Inc.	31722-636	31722-0636-3031722-0636-3131722-0636-90+1 more
Silodosin	Silodosin 4 mg/1	CapsuleOral	Alembic Pharmaceuticals Limited	46708-405	46708-0405-3046708-0405-9046708-0405-91
Silodosin	Silodosin 8 mg/1	CapsuleOral	Alembic Pharmaceuticals Limited	46708-406	46708-0406-3046708-0406-9046708-0406-91

All 29 Silodosin NDCs

Other NDCs under ANDA 211166

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

FDA NDC Directory listings under ANDA 211166
Product	Strength	Form · route	Labeler	Product NDC
Silodosin	Silodosin 4 mg/1	CapsuleOral	Macleods Pharmaceuticals Limited	33342-384
Silodosin	Silodosin 8 mg/1	CapsuleOral	Macleods Pharmaceuticals Limited	33342-385