Cyclobenzaprine Hydrochloride
- Product NDC
- 68071-4826
- 11-digit product format
- 680714826
- Labeler code
- 68071
- Product ID
- 68071-4826_bb8fe075-851d-9c39-e053-2a95a90a7b03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4826-4 | 68071482604 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-4826-4) | 2019-03-29 | 0000-00-00 | No | No | Current |