Cyclobenzaprine Hydrochloride
- Product NDC
- 70938-003
- 11-digit product format
- 709380003
- Labeler code
- 70938
- Product ID
- 70938-003_96c8d48b-d824-6a84-e053-2995a90a0874
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- 1 Veterans Health
- Application
- ANDA078048
- Marketing category
- ANDA
- Marketing start
- 2014-07-31
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record