CYCLOBENZAPRINE HYDROCHLORIDE
- Product NDC
- 60760-363
- 11-digit product format
- 607600363
- Labeler code
- 60760
- Product ID
- 60760-363_960ecca3-1f56-71ae-e053-2a95a90acfc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA208170
- Marketing category
- ANDA
- Marketing start
- 2019-10-24
- 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
- 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 |
|---|
| 60760-363-60 | 60760036360 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-363-60) | 2019-10-24 | 0000-00-00 | No | No | Current |
| 60760-363-90 | 60760036390 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-363-90) | 2019-10-24 | 0000-00-00 | No | No | Current |
| 60760-363-92 | 60760036392 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-363-92) | 2019-10-24 | 0000-00-00 | No | No | Current |