Prescription drug · NDA AUTHORIZED GENERIC

Methylphenidate Hydrochloride NDC 42858-078

Methylphenidate hydrochloride 30 mg/1 · Capsule, Extended release · Oral · Rhodes Pharmaceuticals LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)42858-078Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42858-0078Add 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
42858-078-454285800784590 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42858-078-45)Marketed from Apr 1, 2020

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 — 30 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 205831
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 42858-078_dd7e2d15-d45e-41dc-9d9a-7b68c229b601SPL ID dd7e2d15-d45e-41dc-9d9a-7b68c229b601

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

N442858007845 followed by a unit qualifier and the quantity

Package 42858-0078-45. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under NDA 205831

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

FDA NDC Directory listings under NDA 205831
ProductStrengthForm · routeLabelerProduct NDC
Methylphenidate HydrochlorideMethylphenidate hydrochloride 20 mg/1Capsule, Extended releaseOralRhodes Pharmaceuticals LLC42858-077
Methylphenidate HydrochlorideMethylphenidate hydrochloride 10 mg/1Capsule, Extended releaseOralRhodes Pharmaceuticals LLC42858-075
Methylphenidate HydrochlorideMethylphenidate hydrochloride 15 mg/1Capsule, Extended releaseOralRhodes Pharmaceuticals LLC42858-076
Methylphenidate HydrochlorideMethylphenidate hydrochloride 50 mg/1Capsule, Extended releaseOralRhodes Pharmaceuticals LLC42858-080
Methylphenidate HydrochlorideMethylphenidate hydrochloride 40 mg/1Capsule, Extended releaseOralRhodes Pharmaceuticals LLC42858-079
Methylphenidate HydrochlorideMethylphenidate hydrochloride 60 mg/1Capsule, Extended releaseOralRhodes Pharmaceuticals LLC42858-081

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Methylphenidate Hydrochloride NDC 42858-078 | Med-Code