# CYCLOBENZAPRINE HYDROCHLORIDE
> **ANDA078722** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDS LTD · Approved 2008-05-12
## Drug
- **FDA Application Number:** ANDA078722
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** CYCLOBENZAPRINE HYDROCHLORIDE
- **Generic name:** CYCLOBENZAPRINE HYDROCHLORIDE
- **Active ingredients:** CYCLOBENZAPRINE HYDROCHLORIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** SUN PHARM INDS LTD
- **Manufacturer:** SA3, LLC
- **First approval:** 2008-05-12
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=078722)
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