Cyclobenzaprine Hydrochloride
- Product NDC
- 55700-696
- 11-digit product format
- 557000696
- Labeler code
- 55700
- Product ID
- 55700-696_9eedf658-4acc-4fdc-90cd-623289732724
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA077797
- Marketing category
- ANDA
- Marketing start
- 2018-11-02
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 5 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
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 |
|---|
| 55700-696-01 | 55700069601 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-696-01) | 2018-11-02 | 0000-00-00 | No | No | Current |
| 55700-696-18 | 55700069618 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-696-18) | 2018-11-02 | 0000-00-00 | No | No | Current |
| 55700-696-30 | 55700069630 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-696-30) | 2018-11-02 | 0000-00-00 | No | No | Current |
| 55700-696-60 | 55700069660 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-696-60) | 2018-11-02 | 0000-00-00 | No | No | Current |
| 55700-696-90 | 55700069690 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-696-90) | 2018-11-02 | 0000-00-00 | No | No | Current |