CYCLOBENZPRINE HCL
- Product NDC
- 61919-414
- 11-digit product format
- 619190414
- Labeler code
- 61919
- Product ID
- 61919-414_cecdd91c-453d-3e85-e053-2995a90a6111
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYCLOBENZPRINE HCL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECTRX
- Application
- ANDA078722
- Marketing category
- ANDA
- Marketing start
- 2019-04-04
- 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
- 2022-12-31
- 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 |
|---|
| 61919-414-60 | 61919041460 | 60 TABLET, FILM COATED in 1 BOTTLE (61919-414-60) | 2019-04-04 | 0000-00-00 | No | No | Current |