CYCLOBENZAPRINE HYDROCHLORIDE
- Product NDC
- 63629-7939
- 11-digit product format
- 636297939
- Labeler code
- 63629
- Product ID
- 63629-7939_773e1741-6f2c-4e10-856d-95c936fc9621
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208170
- Marketing category
- ANDA
- Marketing start
- 2017-05-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7939-1 | 63629793901 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7939-1) | 2019-03-15 | 0000-00-00 | No | No | Current |