Fexmid
- Product NDC
- 71205-059
- 11-digit product format
- 712050059
- Labeler code
- 71205
- Product ID
- 71205-059_f716527d-6aaf-458a-9d2a-db3294b3c700
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA071611
- Marketing category
- ANDA
- Marketing start
- 2018-04-30
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 8 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-059 | FEXMID (CYCLOBENZAPRINE HYDROCHLORIDE) TABLET, FILM COATED [PROFICIENT RX LP] | 7 | Legacy NDC | 20220626_2ca861a8-bbb2-4abb-95ba-054cfe825b5a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-059-14 | 71205005914 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-059-14) | 2022-01-05 | 0000-00-00 | No | No | Current |
| 71205-059-20 | 71205005920 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-059-20) | 2019-03-01 | 0000-00-00 | No | No | Current |
| 71205-059-30 | 71205005930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-059-30) | 2018-06-01 | 0000-00-00 | No | No | Current |
| 71205-059-60 | 71205005960 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-059-60) | 2018-06-01 | 0000-00-00 | No | No | Current |
| 71205-059-72 | 71205005972 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-059-72) | 2018-06-01 | 0000-00-00 | No | No | Current |
| 71205-059-90 | 71205005990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-059-90) | 2018-06-01 | 0000-00-00 | No | No | Current |