CYCLOBENZAPRINE HYDROCHLORIDE
- Product NDC
- 71335-1178
- 11-digit product format
- 713351178
- Labeler code
- 71335
- Product ID
- 71335-1178_0f6fab39-134a-4041-ba25-90c721e866b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYCLOBENZAPRINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078218
- Marketing category
- ANDA
- Marketing start
- 2010-02-18
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 10 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1178-1 | 71335117801 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1178-1) | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1178-2 | 71335117802 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1178-2) | 2019-04-05 | 0000-00-00 | No | No | Current |