Cyclobenzaprine Hydrochloride
- Product NDC
- 0904-7809
- 11-digit product format
- 009047809
- Labeler code
- 0904
- Product ID
- 0904-7809_27807fe8-7aa2-43c1-8906-bcea7537f16b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA071611
- Marketing category
- ANDA
- Marketing start
- 1988-02-29
- 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
- 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 |
|---|
| 0904-7809-60 | 00904780960 | 100 TABLET, FILM COATED in 1 BOTTLE (0904-7809-60) | | 1988-02-29 | 0000-00-00 | No | No | Current |
| 0904-7809-61 | 00904780961 | 100 BLISTER PACK in 1 CARTON (0904-7809-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 1988-02-29 | 0000-00-00 | No | No | Current |