What is NDC 71205-888?

71205-888 is the product NDC for Selegiline Hydrochloride, Selegiline hydrochloride 5 mg/1 capsule, listed with the FDA by Proficient Rx LP. It has 6 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 Selegiline Hydrochloride?

12 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Selegiline Hydrochloride NDC 71205-888

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-888Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0888Add 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
71205-888-00	71205088800	100 CAPSULE in 1 BOTTLE (71205-888-00)Marketed from Aug 3, 2021
71205-888-11	71205088811	1000 CAPSULE in 1 BOTTLE (71205-888-11)Marketed from Aug 3, 2021
71205-888-30	71205088830	30 CAPSULE in 1 BOTTLE (71205-888-30)Marketed from Aug 3, 2021
71205-888-55	71205088855	500 CAPSULE in 1 BOTTLE (71205-888-55)Marketed from Aug 3, 2021
71205-888-60	71205088860	60 CAPSULE in 1 BOTTLE (71205-888-60)Marketed from Aug 3, 2021
71205-888-90	71205088890	90 CAPSULE in 1 BOTTLE (71205-888-90)Marketed from Aug 3, 2021

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): Selegiline Hydrochloride
Generic name (nonproprietary): selegiline hydrochloride
Active ingredients: Selegiline hydrochloride — 5 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 206803
Marketing start: Apr 2, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Monoamine Oxidase Inhibitors (Mechanism)Monoamine Oxidase-B Inhibitors (Mechanism)
Identifiers: Product ID 71205-888_a8be3ead-1645-4f63-8683-46e29fdb3041SPL ID a8be3ead-1645-4f63-8683-46e29fdb3041SPL set ID 57b564ef-c89b-4cf6-a11f-f67391d74e7eRxCUI 859186UNII 6W731X367QUPC 0371205888305
Pharmacologic class: Monoamine Oxidase Inhibitor; Monoamine Oxidase Type B Inhibitor

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

N471205088800 followed by a unit qualifier and the quantity

Package 71205-0888-00. 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 Apr 1, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Selegiline capsules, USP are indicated as an adjunct in the management of Parkinsonian patients being treated with levodopa/carbidopa who exhibit deterioration in the quality of their response to this therapy. There is no evidence from controlled studies that selegiline has any beneficial effect in the absence of concurrent levodopa therapy. Evidence supporting this claim was obtained in randomized controlled clinical investigations that compared the effects of added selegiline or placebo in patients receiving levodopa/carbidopa. Selegiline was significantly superior to placebo on all three principal outcome measures employed: change from baseline in daily levodopa/carb…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-888

What is NDC 71205-888?: 71205-888 is the product NDC for Selegiline Hydrochloride, Selegiline hydrochloride 5 mg/1 capsule, listed with the FDA by Proficient Rx LP. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Selegiline Hydrochloride.
What is the active ingredient?: Selegiline 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 Selegiline Hydrochloride?: 12 other product NDCs are listed under this name. See all Selegiline 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 Selegiline Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	TabletOral	A2A Integrated Pharmaceuticals	73141-006	73141-0006-02
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	TabletOral	i3 Pharmaceuticals, LLC	72319-006	72319-0006-02
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Marlex Pharmaceuticals, Inc.	10135-737	10135-0737-60
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Novitium Pharma LLC	70954-504	70954-0504-1070954-0504-20
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2676	71335-2676-01
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2673	71335-2673-01
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	16571-659	16571-0659-0616571-0659-50
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Apotex Corp.	60505-0055	60505-0055-0160505-0055-0260505-0055-03
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	TabletOral	A-S Medication Solutions	50090-2918	50090-2918-00
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	TabletOral	Apotex Corp.	60505-3438	60505-3438-0360505-3438-08

All 13 Selegiline Hydrochloride NDCs

Other NDCs under ANDA 206803

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

FDA NDC Directory listings under ANDA 206803
Product	Strength	Form · route	Labeler	Product NDC
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2673
Selegiline Hydrochloride	Selegiline hydrochloride 5 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	16571-659