Cyclobenzaprine Hydrochloride
- Product NDC
- 60760-399
- 11-digit product format
- 607600399
- Labeler code
- 60760
- Product ID
- 60760-399_7a7fbe99-21b8-10fd-e053-2a91aa0a140d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA077797
- Marketing category
- ANDA
- Marketing start
- 2017-03-30
- 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
- 2020-12-31
- 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 |
|---|
| 60760-399-04 | 60760039904 | 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-399-04) | 2018-03-05 | 0000-00-00 | No | No | Current |
| 60760-399-10 | 60760039910 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-399-10) | 2018-03-05 | 0000-00-00 | No | No | Current |
| 60760-399-15 | 60760039915 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-399-15) | 2017-11-28 | 0000-00-00 | No | No | Current |
| 60760-399-30 | 60760039930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-399-30) | 2017-11-28 | 0000-00-00 | No | No | Current |
| 60760-399-90 | 60760039990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-399-90) | 2018-03-28 | 0000-00-00 | No | No | Current |