CYCLOBENZAPRINE HYDROCHLORIDE
- Product NDC
- 71335-1293
- 11-digit product format
- 713351293
- Labeler code
- 71335
- Product ID
- 71335-1293_f69c85b0-d67e-43aa-b12b-76d1e3f5be1c
- 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
- 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 |
|---|
| 71335-1293-1 | 71335129301 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1293-1) | 2017-05-31 | 0000-00-00 | No | No | Current |
| 71335-1293-2 | 71335129302 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1293-2) | 2017-05-31 | 0000-00-00 | No | No | Current |