What is NDC 70010-006?

70010-006 is the product NDC for Dexmethylphenidate Hydrochloride, Dexmethylphenidate hydrochloride 15 mg/1 capsule, extended release, listed with the FDA by Granules Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Granules Pharmaceuticals Inc., NDC labeler code 70010. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dexmethylphenidate Hydrochloride?

72 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dexmethylphenidate Hydrochloride NDC 70010-006

NDC codes

FDA NDC Directory

Product NDC (as listed)70010-006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70010-0006Add 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	Copy
70010-006-01	7001000060170010000601	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-006-01)Marketed from Dec 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): Dexmethylphenidate Hydrochloride
Generic name (nonproprietary): dexmethylphenidate hydrochloride
Active ingredients: Dexmethylphenidate hydrochloride — 15 mg/1
Dosage form: Capsule, Extended release
Route: Oral
Labeler: Granules Pharmaceuticals Inc.NDC labeler code 70010
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213813
Marketing start: Dec 1, 2020
Listing expires: Dec 31, 2027
DEA schedule: CII
Other FDA classes: Central Nervous System Stimulation (Physiologic effect)
Identifiers: Product ID 70010-006_5d4e3549-d093-0608-e063-6394a90aee16SPL ID 5d4e3549-d093-0608-e063-6394a90aee16
Pharmacologic class: Central Nervous System Stimulant

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

N470010000601 followed by a unit qualifier and the quantity

Package 70010-0006-01. 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

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

About NDC 70010-006

What is NDC 70010-006?: 70010-006 is the product NDC for Dexmethylphenidate Hydrochloride, Dexmethylphenidate hydrochloride 15 mg/1 capsule, extended release, listed with the FDA by Granules Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dexmethylphenidate Hydrochloride.
What is the active ingredient?: Dexmethylphenidate hydrochloride.
Who is the labeler?: Granules Pharmaceuticals Inc., NDC labeler code 70010. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dexmethylphenidate Hydrochloride?: 72 other product NDCs are listed under this name. See all Dexmethylphenidate 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 Dexmethylphenidate Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2426	72162-2426-0172162-2426-06
Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2427	72162-2427-01
Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride 5 mg/1	TabletOral	Nivagen Pharmaceuticals, Inc.	75834-327	75834-0327-01
Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride 10 mg/1	TabletOral	Nivagen Pharmaceuticals, Inc.	75834-328	75834-0328-01
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 5 mg/1	Capsule, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-229	31722-0229-01
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 10 mg/1	Capsule, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-230	31722-0230-01
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 15 mg/1	Capsule, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-231	31722-0231-01
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 20 mg/1	Capsule, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-232	31722-0232-01
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 25 mg/1	Capsule, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-233	31722-0233-01
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 30 mg/1	Capsule, Extended releaseOral	Camber Pharmaceuticals, Inc.	31722-234	31722-0234-01

All 73 Dexmethylphenidate Hydrochloride NDCs

Other NDCs under ANDA 213813

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

FDA NDC Directory listings under ANDA 213813
Product	Strength	Form · route	Labeler	Product NDC
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 5 mg/1	Capsule, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-004
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 10 mg/1	Capsule, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-005
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 20 mg/1	Capsule, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-007
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 25 mg/1	Capsule, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-008
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 30 mg/1	Capsule, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-009
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 35 mg/1	Capsule, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-010
Dexmethylphenidate Hydrochloride	Dexmethylphenidate hydrochloride 40 mg/1	Capsule, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-011