Tamsulosin Hydrochloride NDC 65841-695

NDC codes

FDA NDC Directory

Product NDC (as listed)65841-695Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65841-0695Add 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
65841-695-01	65841069501	100 CAPSULE in 1 BOTTLE (65841-695-01)Marketed from Apr 27, 2010
65841-695-05	65841069505	500 CAPSULE in 1 BOTTLE (65841-695-05)Marketed from Apr 27, 2010
65841-695-06	65841069506	30 CAPSULE in 1 BOTTLE (65841-695-06)Marketed from Apr 27, 2010
65841-695-10	65841069510	1000 CAPSULE in 1 BOTTLE (65841-695-10)Marketed from Apr 27, 2010
65841-695-14	65841069514	60 CAPSULE in 1 BOTTLE (65841-695-14)Marketed from Apr 27, 2010
65841-695-16	65841069516	90 CAPSULE in 1 BOTTLE (65841-695-16)Marketed from Apr 27, 2010
65841-695-77	65841069577	10 BLISTER PACK in 1 CARTON (65841-695-77) / 10 CAPSULE in 1 BLISTER PACKMarketed from Apr 27, 2010

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
Labeler: Zydus Lifesciences Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078225
Marketing start: Apr 27, 2010
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 65841-695_b05d1829-8334-4145-b49d-6074624bc499SPL ID b05d1829-8334-4145-b49d-6074624bc499SPL set ID 276c7e26-f86a-46b9-b626-ceef76b729a4RxCUI 863669UNII 11SV1951MR
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

N465841069501 followed by a unit qualifier and the quantity

Package 65841-0695-01. 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 Aug 12, 2024.

Full label on DailyMed (opens in a new tab)

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
Product	Strength	Form · route	Labeler	Product NDC
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	American Health Packaging	68084-299
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-4346
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Zydus Pharmaceuticals USA Inc.	68382-132
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Coupler LLC	67046-1015
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-2142
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-4145
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Aphena Pharma Solutions - Tennessee, LLC	71610-724
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Quallent Pharmaceuticals Health LLC	82009-025