Cyclobenzaprine Hydrochloride
- Product NDC
- 63629-8983
- 11-digit product format
- 636298983
- Labeler code
- 63629
- Product ID
- 63629-8983_043fff25-ff13-4bcc-8483-baf71e78c298
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077797
- Marketing category
- ANDA
- Marketing start
- 2017-03-30
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8983-1 | 63629898301 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-8983-1) | 2021-12-07 | 0000-00-00 | No | No | Current |