NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2430Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2430Add 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
72162-2430-17216224300172162243001100 TABLET in 1 BOTTLE (72162-2430-1)Marketed from Nov 18, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Methylphenidate Hydrochloride
Generic name (nonproprietary)
methylphenidate hydrochloride
Active ingredients
Methylphenidate hydrochloride — 20 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208737
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 72162-2430_3cf7fbf3-8b3d-404e-b987-6302f6510ddaSPL ID 3cf7fbf3-8b3d-404e-b987-6302f6510ddaSPL set ID c87a2000-b75c-41df-8497-7e00a9b41ad4RxCUI 1091392UNII 4B3SC438HI

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

N472162243001 followed by a unit qualifier and the quantity

Package 72162-2430-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Methylphenidate hydrochloride tablets are indicated for the treatment of: • Attention Deficit Hyperactivity Disorders (ADHD) in pediatric patients 6 years and older and adults • Narcolepsy Methylphenidate hydrochloride tablets are a central nervous system (CNS) stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorders (ADHD) and Narcolepsy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2430

What is NDC 72162-2430?
72162-2430 is the product NDC for Methylphenidate Hydrochloride, Methylphenidate hydrochloride 20 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Methylphenidate Hydrochloride.
What is the active ingredient?
Methylphenidate hydrochloride.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Methylphenidate Hydrochloride?
148 other product NDCs are listed under this name. See all Methylphenidate 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 Methylphenidate Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Methylphenidate HydrochlorideMethylphenidate hydrochloride 72 mg/1Tablet, Extended releaseOralNorthstar Rx LLC72603-39972603-0399-01
Methylphenidate HydrochlorideMethylphenidate hydrochloride 72 mg/1Tablet, Extended releaseOralSun Pharmaceutical Industries, Inc.57664-71057664-0710-8357664-0710-88
Methylphenidate HydrochlorideMethylphenidate hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-296871335-2968-01
Methylphenidate HydrochlorideMethylphenidate hydrochloride 5 mg/1TabletOralNivagen Pharmaceuticals, Inc.75834-32475834-0324-01
Methylphenidate HydrochlorideMethylphenidate hydrochloride 10 mg/1TabletOralNivagen Pharmaceuticals, Inc.75834-32575834-0325-01
Methylphenidate HydrochlorideMethylphenidate hydrochloride 20 mg/1TabletOralNivagen Pharmaceuticals, Inc.75834-32675834-0326-01
Methylphenidate HydrochlorideMethylphenidate hydrochloride 5 mg/1TabletOralBryant Ranch Prepack72162-242872162-2428-01
Methylphenidate HydrochlorideMethylphenidate hydrochloride 10 mg/1TabletOralBryant Ranch Prepack72162-242972162-2429-01
Methylphenidate HydrochlorideMethylphenidate hydrochloride 63 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-70013811-0700-30
Methylphenidate HydrochlorideMethylphenidate hydrochloride 45 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-71113811-0711-30

All 149 Methylphenidate Hydrochloride NDCs

Other NDCs under ANDA 208737

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

FDA NDC Directory listings under ANDA 208737
ProductStrengthForm · routeLabelerProduct NDC
Methylphenidate HydrochlorideMethylphenidate hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-2968
Methylphenidate HydrochlorideMethylphenidate hydrochloride 5 mg/1TabletOralBryant Ranch Prepack72162-2428
Methylphenidate HydrochlorideMethylphenidate hydrochloride 10 mg/1TabletOralBryant Ranch Prepack72162-2429
Methylphenidate HydrochlorideMethylphenidate hydrochloride 5 mg/1TabletOralNivagen Pharmaceuticals, Inc.75834-324
Methylphenidate HydrochlorideMethylphenidate hydrochloride 10 mg/1TabletOralNivagen Pharmaceuticals, Inc.75834-325
Methylphenidate HydrochlorideMethylphenidate hydrochloride 20 mg/1TabletOralNivagen Pharmaceuticals, Inc.75834-326

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