NDC codes

FDA NDC Directory
Product NDC (as listed)0115-8211Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00115-8211Add 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
0115-8211-0100115821101100 CAPSULE in 1 BOTTLE (0115-8211-01)Marketed from Apr 1, 2025

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Tamsulosin Hydrochloride
Generic name (nonproprietary)
tamsulosin hydrochloride
Active ingredients
Tamsulosin hydrochloride — .4 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Amneal Pharmaceuticals of New York LLCNDC labeler code 0115
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090377
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)
Identifiers
Product ID 0115-8211_e62d078e-2896-4acd-bcaa-c21e855e66e1SPL ID e62d078e-2896-4acd-bcaa-c21e855e66e1SPL set ID c3ae55dd-6a0e-4f3a-82b6-2448e0545550RxCUI 863669UNII 11SV1951MRUPC 0301158211011
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

N400115821101 followed by a unit qualifier and the quantity

Package 00115-8211-01. 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 .

Indications (excerpt from the label)

Tamsulosin hydrochloride capsules are indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH) [see Clinical Studies (14) ] . Tamsulosin hydrochloride capsules are not indicated for the treatment of hypertension. Tamsulosin hydrochloride is an alpha 1 adrenoceptor antagonist indicated for treatment of the signs and symptoms of benign prostatic hyperplasia ( 1 ) Tamsulosin hydrochloride 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 0115-8211

What is NDC 0115-8211?
0115-8211 is the product NDC for Tamsulosin Hydrochloride, Tamsulosin hydrochloride .4 mg/1 capsule, listed with the FDA by Amneal Pharmaceuticals of New York LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Tamsulosin Hydrochloride.
What is the active ingredient?
Tamsulosin hydrochloride.
Who is the labeler?
Amneal Pharmaceuticals of New York LLC, NDC labeler code 0115. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tamsulosin Hydrochloride?
60 other product NDCs are listed under this name. See all Tamsulosin Hydrochloride 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 Tamsulosin Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-414568788-4145-0168788-4145-0368788-4145-06+2 more
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralCoupler LLC67046-101567046-1015-03
tamsulosin hydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralXLCare Pharmaceuticals, Inc.72865-35072865-0350-0572865-0350-90
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralAvKARE42291-98942291-0989-1042291-0989-90
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralCardinal Health 107, LLC55154-214255154-2142-00
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralCardinal Health 107, LLC55154-263655154-2636-00
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralXLCare Pharmaceuticals, Inc72865-28272865-0282-0172865-0282-0572865-0282-90
Tamsulosin hydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-91071610-0910-3071610-0910-5371610-0910-60+2 more
Tamsulosin hydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralEXELAN PHARMACEUTICALS, INC.76282-74476282-0744-0576282-0744-90
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralQuallent Pharmaceuticals Health LLC82009-02582009-0025-10

All 61 Tamsulosin Hydrochloride NDCs

Other NDCs under ANDA 090377

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

FDA NDC Directory listings under ANDA 090377
ProductStrengthForm · routeLabelerProduct NDC
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralAvKARE42291-989

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