NDC codes

FDA NDC Directory
Product NDC (as listed)60429-176Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60429-0176Add 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
60429-176-60604290176606042901766060 TABLET in 1 BOTTLE (60429-176-60)Marketed from Apr 2, 2013

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
Tablet
Route
Oral
Labeler
Golden State Medical Supply, Inc.NDC labeler code 60429
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074871
Marketing start
Listing expires
Other FDA classes
Monoamine Oxidase Inhibitors (Mechanism)Monoamine Oxidase-B Inhibitors (Mechanism)
Identifiers
Product ID 60429-176_445cd6b2-2a0f-5f90-e063-6294a90ab877SPL ID 445cd6b2-2a0f-5f90-e063-6294a90ab877SPL set ID 040a97e5-efd1-4a2f-b737-2f13e5366d70RxCUI 859193UNII 6W731X367Q
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

N460429017660 followed by a unit qualifier and the quantity

Package 60429-0176-60. 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)

INDICATIONS AND USAGE Selegiline Hydrochloride Tablets 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 l…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60429-176

What is NDC 60429-176?
60429-176 is the product NDC for Selegiline Hydrochloride, Selegiline hydrochloride 5 mg/1 tablet, listed with the FDA by Golden State Medical Supply, Inc.. It has 1 package NDC, 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?
Golden State Medical Supply, Inc., NDC labeler code 60429. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1TabletOralA2A Integrated Pharmaceuticals73141-00673141-0006-02
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1TabletOrali3 Pharmaceuticals, LLC72319-00672319-0006-02
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1CapsuleOralMarlex Pharmaceuticals, Inc.10135-73710135-0737-60
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1CapsuleOralNovitium Pharma LLC70954-50470954-0504-1070954-0504-20
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1CapsuleOralBryant Ranch Prepack71335-267671335-2676-01
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-65916571-0659-0616571-0659-50
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1CapsuleOralProficient Rx LP71205-88871205-0888-0071205-0888-1171205-0888-30+3 more
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1CapsuleOralBryant Ranch Prepack71335-267371335-2673-01
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1CapsuleOralApotex Corp.60505-005560505-0055-0160505-0055-0260505-0055-03
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1TabletOralA-S Medication Solutions50090-291850090-2918-00

All 13 Selegiline Hydrochloride NDCs

Other NDCs under ANDA 074871

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

FDA NDC Directory listings under ANDA 074871
ProductStrengthForm · routeLabelerProduct NDC
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1TabletOralA-S Medication Solutions50090-2918
Selegiline HydrochlorideSelegiline hydrochloride 5 mg/1TabletOralApotex Corp.60505-3438

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