Cyclobenzaprine Hydrochloride
- Product NDC
- 72162-1359
- 11-digit product format
- 721621359
- Labeler code
- 72162
- Product ID
- 72162-1359_720a5d84-521d-4a0f-a37b-cc0a6c7f2217
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077797
- Marketing category
- ANDA
- Marketing start
- 2017-03-30
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0VE05JYS2P | CYCLOBENZAPRINE HYDROCHLORIDE | 6202-23-9 | CYCLOBENZAPRINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1359-0 | 72162135900 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-0) | 2024-01-31 | No | No | Historical |
| 72162-1359-1 | 72162135901 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-1) | 2024-01-31 | No | No | Historical |
| 72162-1359-5 | 72162135905 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-5) | 2024-01-31 | No | No | Historical |