Cyclobenzaprine Hydrochloride
- Product NDC
- 72789-188
- 11-digit product format
- 727890188
- Labeler code
- 72789
- Product ID
- 72789-188_c1a9ff0f-2954-76a2-e053-2a95a90a562b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078048
- Marketing category
- ANDA
- Marketing start
- 2014-07-31
- 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
- 2022-12-31
- 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 |
|---|
| 72789-188-09 | 72789018809 | 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-188-09) | 2021-05-05 | 0000-00-00 | No | No | Current |