Cymbalta 60 mg/1
Duloxetine hydrochloride · CAPSULE, DELAYED RELEASE · Eli Lilly and Company
Cymbalta is a capsule, delayed release containing duloxetine hydrochloride at 60 mg/1, taken oral. Manufactured by Eli Lilly and Company.
Key Facts
- Brand Name
- Cymbalta
- Generic Name
- Duloxetine hydrochloride
- NDC Code (Product)
0002-3270- Manufacturer
- Eli Lilly and Company
- Strength
- 60 mg/1
- Dosage Form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA021427
- Marketing Start
- 01/15/2010
Recall History
No Recall HistoryFrequently Asked Questions
What is Cymbalta used for?
Cymbalta contains Duloxetine hydrochloride. It is a capsule, delayed release taken oral. Consult your doctor for specific uses.
Is Cymbalta a controlled substance?
Cymbalta is not classified as a controlled substance by the DEA.
What is the generic name for Cymbalta?
The generic name for Cymbalta is Duloxetine hydrochloride. There are 11 other brand versions of Duloxetine hydrochloride.
What is the NDC code for Cymbalta 60 mg/1?
The NDC (National Drug Code) for Cymbalta 60 mg/1 is 0002-3270, listed by Eli Lilly and Company.
Product NDC
0002-3270
Other Cymbalta Dosages
Other Duloxetine Brands
See all →- Duloxetine Delayed-Release60 mg/172162-1599
- Duloxetine60 mg/182009-032
- Duloxetine Delayed-Release30 mg/150090-3205
- Duloxetine Delayed-Release60 mg/163629-1992
- Duloxetine Delayed-Release30 mg/151991-747
- Duloxetine60 mg/160687-745
- Duloxetine Delayed-Release20 mg/163629-1990
- Duloxetine30 mg/171610-402
- Duloxetine20 mg/182009-029
- DULOXETINE HYDROCHLORIDE20 mg/150771-201
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)