CYCLOBENZAPRINE HYDROCHLORIDE
- Product NDC
- 63629-7960
- 11-digit product format
- 636297960
- Labeler code
- 63629
- Product ID
- 63629-7960_a428f15e-8728-4433-b8e3-193eb72bec17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYCLOBENZAPRINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078218
- Marketing category
- ANDA
- Marketing start
- 2010-02-18
- 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
- 2023-12-31
- 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 |
|---|
| 63629-7960-1 | 63629796001 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-7960-1) | 2019-03-13 | 0000-00-00 | No | No | Current |
| 63629-7960-2 | 63629796002 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7960-2) | 2019-03-13 | 0000-00-00 | No | No | Current |