AKTEN 35 mg/mL
LIDOCAINE HYDROCHLORIDE ANHYDROUS · GEL · Thea Pharma Inc.
No Recall HistoryCurrently in Shortage
Plain English
AKTEN is a gel containing lidocaine hydrochloride anhydrous at 35 mg/mL, taken ophthalmic. Manufactured by Thea Pharma Inc..
Key Facts
- Brand Name
- AKTEN
- Generic Name
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- NDC Code (Product)
82584-792- Manufacturer
- Thea Pharma Inc.
- Strength
- 35 mg/mL
- Dosage Form
- GEL
- Route
- OPHTHALMIC
- Marketing Status
- Application #
- NDA022221
- Marketing Start
- 12/01/2022
Recall History
No Recall HistoryFrequently Asked Questions
What is AKTEN used for?
AKTEN contains LIDOCAINE HYDROCHLORIDE ANHYDROUS. It is a gel taken ophthalmic. Consult your doctor for specific uses.
Is AKTEN a controlled substance?
AKTEN is not classified as a controlled substance by the DEA.
What is the generic name for AKTEN?
The generic name for AKTEN is LIDOCAINE HYDROCHLORIDE ANHYDROUS. There are 8 other brand versions of LIDOCAINE HYDROCHLORIDE ANHYDROUS.
What is the NDC code for AKTEN 35 mg/mL?
The NDC (National Drug Code) for AKTEN 35 mg/mL is 82584-792, listed by Thea Pharma Inc..
Other Lidocaine Brands
See all →- Lidocaine Hydrochloride10 mg/mL85766-187
- Lidocaine Hydrochloride and Dextrose5 g/100mL84549-594
- Lidocaine Hydrochloride and Dextrose5 g/100mL0264-9594
- Lidocaine Hydrochloride10 mg/mL0404-9888
- Lidocaine Hydrochloride and Dextrose5 g/100mL0264-9598
- Lidocaine Hydrochloride20 mg/mL0404-9895
- Lidocaine Hydrochloride10 mg/mL0404-9887
- Lidocaine Hydrochloride10 mg/mL65282-1605
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)