Cyclobenzaprine Hydrochloride
- Product NDC
- 63629-7653
- 11-digit product format
- 636297653
- Labeler code
- 63629
- Product ID
- 63629-7653_7970ec53-6323-4d2a-8aab-ec02f3e5847f
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7653-1 | 63629765301 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-7653-1) | 2010-02-18 | 0000-00-00 | No | No | Current |
| 63629-7653-2 | 63629765302 | 15 TABLET, FILM COATED in 1 BOTTLE (63629-7653-2) | 2010-02-18 | 0000-00-00 | No | No | Current |