NDC codes

FDA NDC Directory
Product NDC (as listed)82009-025Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82009-0025Add 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
82009-025-10820090025101000 CAPSULE in 1 BOTTLE (82009-025-10)Marketed from Aug 20, 2022

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)
Tamsulosin Hydrochloride
Generic name (nonproprietary)
tamsulosin hydrochloride
Active ingredients
Tamsulosin hydrochloride.4 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078225
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)
Identifiers
Product ID 82009-025_82b44507-051f-4892-a0b7-ed3955c2f72fSPL ID 82b44507-051f-4892-a0b7-ed3955c2f72fSPL set ID 12ba3063-a134-41e2-8447-45933d4f0f58RxCUI 863669UNII 11SV1951MRUPC 0382009025100
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

N482009002510 followed by a unit qualifier and the quantity

Package 82009-0025-10. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 078225

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

FDA NDC Directory listings under ANDA 078225
ProductStrengthForm · routeLabelerProduct NDC
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralZydus Lifesciences Limited65841-695
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralAmerican Health Packaging68084-299
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralBryant Ranch Prepack63629-4346
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.68382-132
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralCoupler LLC67046-1015
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralCardinal Health 107, LLC55154-2142
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-4145
Tamsulosin HydrochlorideTamsulosin hydrochloride .4 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-724

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