What is NDC 71205-217?

71205-217 is the product NDC for Tamsulosin Hydrochloride, Tamsulosin hydrochloride .4 mg/1 capsule, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. 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?

61 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tamsulosin Hydrochloride NDC 71205-217

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-217Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0217Add 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
71205-217-07	7120502170771205021707	7 CAPSULE in 1 BOTTLE (71205-217-07)Marketed from Aug 11, 2017
71205-217-14	7120502171471205021714	14 CAPSULE in 1 BOTTLE (71205-217-14)Marketed from Feb 5, 2020
71205-217-30	7120502173071205021730	30 CAPSULE in 1 BOTTLE (71205-217-30)Marketed from Aug 11, 2017
71205-217-60	7120502176071205021760	60 CAPSULE in 1 BOTTLE (71205-217-60)Marketed from Aug 11, 2017
71205-217-90	7120502179071205021790	90 CAPSULE in 1 BOTTLE (71205-217-90)Marketed from Aug 11, 2017

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: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207405
Marketing start: Aug 11, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 71205-217_668d5539-1561-457c-9a7c-38784a9b5c66SPL ID 668d5539-1561-457c-9a7c-38784a9b5c66SPL set ID 06b44e53-c6e7-4e12-a8fd-572d092cfa70RxCUI 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

N471205021707 followed by a unit qualifier and the quantity

Package 71205-0217-07. 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 Feb 1, 2020.

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 Capsules 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 71205-217

What is NDC 71205-217?: 71205-217 is the product NDC for Tamsulosin Hydrochloride, Tamsulosin hydrochloride .4 mg/1 capsule, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, 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?: Proficient Rx LP, NDC labeler code 71205. 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?: 61 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-4145	68788-4145-0168788-4145-0368788-4145-06+2 more
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Coupler LLC	67046-1015	67046-1015-03
tamsulosin hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	XLCare Pharmaceuticals, Inc.	72865-350	72865-0350-0572865-0350-90
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	AvKARE	42291-989	42291-0989-1042291-0989-90
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Amneal Pharmaceuticals of New York LLC	0115-8211	00115-8211-01
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-2142	55154-2142-00
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-2636	55154-2636-00
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	XLCare Pharmaceuticals, Inc	72865-282	72865-0282-0172865-0282-0572865-0282-90
Tamsulosin hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Aphena Pharma Solutions - Tennessee, LLC	71610-910	71610-0910-3071610-0910-5371610-0910-60+2 more
Tamsulosin hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	EXELAN PHARMACEUTICALS, INC.	76282-744	76282-0744-0576282-0744-90

All 62 Tamsulosin Hydrochloride NDCs

Other NDCs under ANDA 207405

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

FDA NDC Directory listings under ANDA 207405
Product	Strength	Form · route	Labeler	Product NDC
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	A-S Medication Solutions	50090-3646
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	A-S Medication Solutions	50090-4906
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	AvPAK	50268-740
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	51407-879
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Chartwell RX, LLC	62135-775
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Ascend Laboratories, LLC	67877-450
Tamsulosin Hydrochloride	Tamsulosin hydrochloride .4 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-1538