NDC codes

FDA NDC Directory
Product NDC (as listed)51407-926Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51407-0926Add 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
51407-926-0151407092601100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51407-926-01)Marketed from Jun 21, 2024

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)
Methylphenidate Hydrochloride
Generic name (nonproprietary)
methylphenidate hydrochloride
Active ingredients
Methylphenidate hydrochloride — 36 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205327
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 51407-926_50289734-e08d-0f5a-e063-6394a90ab421SPL ID 50289734-e08d-0f5a-e063-6394a90ab421SPL set ID 22e5ddfa-7264-fbb1-e063-6394a90a6483RxCUI 1091155, 1091170, 1091185, 1091210UNII 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

N451407092601 followed by a unit qualifier and the quantity

Package 51407-0926-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 205327

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

FDA NDC Directory listings under ANDA 205327
ProductStrengthForm · routeLabelerProduct NDC
Methylphenidate HydrochlorideMethylphenidate hydrochloride 27 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-707
Methylphenidate HydrochlorideMethylphenidate hydrochloride 18 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-706
Methylphenidate HydrochlorideMethylphenidate hydrochloride 72 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-710
Methylphenidate HydrochlorideMethylphenidate hydrochloride 36 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-708
Methylphenidate HydrochlorideMethylphenidate hydrochloride 54 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-709
Methylphenidate HydrochlorideMethylphenidate hydrochloride 27 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-925
Methylphenidate HydrochlorideMethylphenidate hydrochloride 18 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-924
Methylphenidate HydrochlorideMethylphenidate hydrochloride 54 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-927

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