Cyclobenzaprine Hydrochloride
- Product NDC
- 70518-0301
- 11-digit product format
- 705180301
- Labeler code
- 70518
- Product ID
- 70518-0301_837a1f25-7648-2a9b-e053-2991aa0abc73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071611
- Marketing category
- ANDA
- Marketing start
- 2017-03-09
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record