Cyclobenzaprine Hydrochloride
- Product NDC
- 55154-8143
- 11-digit product format
- 551548143
- Labeler code
- 55154
- Product ID
- 55154-8143_6f6db226-c5a8-4a9e-b31c-0d6113a59b9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077797
- Marketing category
- ANDA
- Marketing start
- 2007-02-28
- 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
- 2021-12-31
- 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 |
|---|
| 55154-8143-0 | 55154814300 | 10 BLISTER PACK in 1 BAG (55154-8143-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2007-02-28 | 0000-00-00 | No | No | Current |