Cyclobenzaprine Hydrochloride
- Product NDC
- 68788-9508
- 11-digit product format
- 687889508
- Labeler code
- 68788
- Product ID
- 68788-9508_20ed0ed9-8933-440d-a9d2-cee520ea9ff6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078048
- Marketing category
- ANDA
- Marketing start
- 2014-02-26
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record