Cyclobenzaprine Hydrochloride
- Product NDC
- 66267-775
- 11-digit product format
- 662670775
- Labeler code
- 66267
- Product ID
- 66267-775_b8a7d31b-81a0-174e-e053-2a95a90a9ed5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090478
- Marketing category
- ANDA
- Marketing start
- 2012-04-02
- 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 |
|---|
| 66267-775-01 | 66267077501 | 10 TABLET in 1 BOTTLE (66267-775-01) | 10 tablet | 2018-01-23 | 0000-00-00 | No | No | Current |
| 66267-775-03 | 66267077503 | 30 TABLET in 1 BOTTLE (66267-775-03) | 30 tablet | 2018-01-23 | 0000-00-00 | No | No | Current |
| 66267-775-04 | 66267077504 | 4 TABLET in 1 BOTTLE (66267-775-04) | 4 tablet | 2018-01-23 | 0000-00-00 | No | No | Current |
| 66267-775-06 | 66267077506 | 6 TABLET in 1 BOTTLE (66267-775-06) | 6 tablet | 2018-01-23 | 0000-00-00 | No | No | Current |
| 66267-775-07 | 66267077507 | 7 TABLET in 1 BOTTLE (66267-775-07) | 7 tablet | 2018-01-23 | 0000-00-00 | No | No | Current |