What is NDC 75907-024?

75907-024 is the product NDC for Clonidine, Clonidine .2 mg/24h patch, extended release, listed with the FDA by Dr. Reddy's Labratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Dr. Reddy's Labratories Inc., NDC labeler code 75907. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Clonidine?

11 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Clonidine NDC 75907-024 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)75907-024Labeler and product segments. Claims need a package NDC.

Product NDC at billing width75907-0024Add 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
75907-024-48	7590700244875907002448	4 POUCH in 1 CARTON (75907-024-48) / 1 PATCH in 1 POUCH (75907-024-11) / 24 h in 1 PATCHMarketed from Feb 10, 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): Clonidine
Generic name (nonproprietary): clonidine
Active ingredients: Clonidine — .2 mg/24h
Dosage form: Patch, Extended release
Route: Transdermal
Labeler: Dr. Reddy's Labratories Inc.NDC labeler code 75907
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 079090
Marketing start: Feb 10, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha2-Agonists (Mechanism)
Identifiers: Product ID 75907-024_07b162a5-9473-c1d7-9cba-aef238255deeSPL ID 07b162a5-9473-c1d7-9cba-aef238255deeSPL set ID a179570b-eef1-176a-820c-5f603d222a60RxCUI 998671, 998675, 998679UNII MN3L5RMN02
Pharmacologic class: Central alpha-2 Adrenergic Agonist

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. Transdermal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N475907002448 followed by a unit qualifier and the quantity

Package 75907-0024-48. 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 Feb 5, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Clonidine transdermal system is indicated in the treatment of hypertension. It may be employed alone or concomitantly with other antihypertensive agents.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 75907-024

What is NDC 75907-024?: 75907-024 is the product NDC for Clonidine, Clonidine .2 mg/24h patch, extended release, listed with the FDA by Dr. Reddy's Labratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Clonidine.
What is the active ingredient?: Clonidine.
Who is the labeler?: Dr. Reddy's Labratories Inc., NDC labeler code 75907. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Clonidine?: 11 other product NDCs are listed under this name. See all Clonidine 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 Clonidine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Clonidine	Clonidine .1 mg/24h	Patch, Extended releaseTransdermal	Dr. Reddy's Labratories Inc.	75907-023	75907-0023-48
Clonidine	Clonidine .3 mg/24h	Patch, Extended releaseTransdermal	Dr. Reddy's Labratories Inc.	75907-025	75907-0025-48
Clonidine	Clonidine .17 mg/1	Tablet, Extended releaseOral	TruPharma, LLC	52817-375	52817-0375-30
Clonidine	Clonidine .17 mg/1	Tablet, Extended releaseOral	PALMETTO PHARMACEUTICALS INC.	68134-603	68134-0603-30
Clonidine	Clonidine hydrochloride .1 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-247	50742-0247-0550742-0247-3050742-0247-60
Clonidine	Clonidine .3 mg/24h	Patch, Extended releaseTransdermal	Mayne Pharma Inc.	51862-455	—
Clonidine	Clonidine hydrochloride 100 ug/mL	Injection, SolutionEpidural	XGen Pharmaceuticals DJB, Inc.	39822-2000	39822-2000-01
Clonidine	Clonidine hydrochloride 500 ug/mL	Injection, SolutionEpidural	XGen Pharmaceuticals DJB, Inc.	39822-2010	39822-2010-01
Clonidine	Clonidine .2 mg/d	PatchTransdermal	Mylan Pharmaceuticals Inc.	0378-0872	00378-0872-99
Clonidine	Clonidine .3 mg/d	PatchTransdermal	Mylan Pharmaceuticals Inc.	0378-0873	00378-0873-99

All 12 Clonidine NDCs

Other NDCs under ANDA 079090

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

FDA NDC Directory listings under ANDA 079090
Product	Strength	Form · route	Labeler	Product NDC
Clonidine	Clonidine .3 mg/24h	Patch, Extended releaseTransdermal	Mayne Pharma Inc.	51862-455
Clonidine	Clonidine .1 mg/24h	Patch, Extended releaseTransdermal	Dr. Reddy's Labratories Inc.	75907-023
Clonidine	Clonidine .3 mg/24h	Patch, Extended releaseTransdermal	Dr. Reddy's Labratories Inc.	75907-025