Clonidine .1 mg/24h
CLONIDINE · PATCH, EXTENDED RELEASE · Dr. Reddy's Labratories Inc.
Clonidine is a patch, extended release containing clonidine at .1 mg/24h, taken transdermal. Manufactured by Dr. Reddy's Labratories Inc..
Key Facts
- Brand Name
- Clonidine
- Generic Name
- CLONIDINE
- NDC Code (Product)
75907-023- Manufacturer
- Dr. Reddy's Labratories Inc.
- Strength
- .1 mg/24h
- Dosage Form
- PATCH, EXTENDED RELEASE
- Route
- TRANSDERMAL
- Marketing Status
- Application #
- ANDA079090
- Drug Class
- Central alpha-2 Adrenergic Agonist [EPC]
- Marketing Start
- 02/10/2024
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is Clonidine used for?
Clonidine contains CLONIDINE. It is a patch, extended release taken transdermal. Consult your doctor for specific uses.
Is Clonidine a controlled substance?
Clonidine is not classified as a controlled substance by the DEA.
What is the generic name for Clonidine?
The generic name for Clonidine is CLONIDINE. There are 12 other brand versions of CLONIDINE.
What is the NDC code for Clonidine .1 mg/24h?
The NDC (National Drug Code) for Clonidine .1 mg/24h is 75907-023, listed by Dr. Reddy's Labratories Inc..
Other Clonidine Brands
See all →- Clonidine Hydrochloride.1 mg/172162-2609
- Clonidine transdermal system.2 mg/d0591-3509
- Clonidine Hydrochloride500 ug/mL0143-9723
- clonidine hydrochloride.2 mg/146708-307
- clonidine hydrochloride.1 mg/150090-5577
- Clonidine Hydrochloride.1 mg/150090-6744
- clonidine hydrochloride.1 mg/150090-7009
- Clonidine hydrochloride.3 mg/151655-451
- Clonidine Transdermal System USP, 0.2 mg/day.2 mg/d52817-611
- Clonidine Transdermal System USP, 0.3 mg/day.3 mg/d52817-612
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)