Cyclobenzaprine Hydrochloride
- Product NDC
- 50090-3728
- 11-digit product format
- 500903728
- Labeler code
- 50090
- Product ID
- 50090-3728_fea01945-eec9-4efb-89e4-128cb33c48e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071611
- Marketing category
- ANDA
- Marketing start
- 1989-05-03
- 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
- 2022-12-31
- 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 |
|---|
| 50090-3728-0 | 50090372800 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-3728-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 33 blister pack | 2018-10-25 | 0000-00-00 | No | No | Current |