Cyclobenzaprine hydrochloride
- Product NDC
- 60760-284
- 11-digit product format
- 607600284
- Labeler code
- 60760
- Product ID
- 60760-284_7a7fe880-0b92-015c-e053-2991aa0a02bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA073541
- Marketing category
- ANDA
- Marketing start
- 2018-05-08
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-284-04 | 60760028404 | 4 TABLET in 1 BOTTLE, PLASTIC (60760-284-04) | 4 tablet | 2018-05-08 | 0000-00-00 | No | No | Current |
| 60760-284-15 | 60760028415 | 15 TABLET in 1 BOTTLE, PLASTIC (60760-284-15) | 15 tablet | 2018-05-08 | 0000-00-00 | No | No | Current |
| 60760-284-30 | 60760028430 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-284-30) | 30 tablet | 2018-05-08 | 0000-00-00 | No | No | Current |