Cyclobenzaprine Hydrochloride
- Product NDC
- 68788-7398
- 11-digit product format
- 687887398
- Labeler code
- 68788
- Product ID
- 68788-7398_866edff0-fe80-4af2-9ea6-bb3cf272e1c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090478
- Marketing category
- ANDA
- Marketing start
- 2016-09-30
- 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
- 2021-12-31
- 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 |
|---|
| 68788-7398-0 | 68788739800 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-7398-0) | 2016-09-30 | 0000-00-00 | No | No | Current |
| 68788-7398-1 | 68788739801 | 14 TABLET, FILM COATED in 1 BOTTLE (68788-7398-1) | 2016-09-30 | 0000-00-00 | No | No | Current |
| 68788-7398-2 | 68788739802 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7398-2) | 2016-09-30 | 0000-00-00 | No | No | Current |
| 68788-7398-3 | 68788739803 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7398-3) | 2016-09-30 | 0000-00-00 | No | No | Current |
| 68788-7398-5 | 68788739805 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-7398-5) | 2016-09-30 | 0000-00-00 | No | No | Current |
| 68788-7398-6 | 68788739806 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7398-6) | 2016-09-30 | 0000-00-00 | No | No | Current |
| 68788-7398-8 | 68788739808 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7398-8) | 2016-09-30 | 0000-00-00 | No | No | Current |
| 68788-7398-9 | 68788739809 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7398-9) | 2016-09-30 | 0000-00-00 | No | No | Current |