Cyclobenzaprine hydrochloride
- Product NDC
- 76420-840
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA213324
- Marketing category
- ANDA
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 76420-840-00 | 1000 TABLET, FILM COATED in 1 BOTTLE (76420-840-00) | 2024-08-16 | | No | Historical |
| 76420-840-01 | 1 TABLET, FILM COATED in 1 BOTTLE (76420-840-01) | 2024-08-16 | | No | Historical |
| 76420-840-02 | 2 TABLET, FILM COATED in 1 BOTTLE (76420-840-02) | 2024-08-16 | | No | Historical |
| 76420-840-07 | 7 TABLET, FILM COATED in 1 BOTTLE (76420-840-07) | 2024-08-16 | | No | Historical |
| 76420-840-10 | 100 TABLET, FILM COATED in 1 BOTTLE (76420-840-10) | 2024-08-16 | | No | Historical |
| 76420-840-20 | 20 TABLET, FILM COATED in 1 BOTTLE (76420-840-20) | 2024-08-16 | | No | Historical |
| 76420-840-30 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-840-30) | 2024-08-16 | | No | Historical |
| 76420-840-60 | 60 TABLET, FILM COATED in 1 BOTTLE (76420-840-60) | 2024-08-16 | | No | Historical |
| 76420-840-90 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-840-90) | 2024-08-16 | | No | Historical |