Cyclobenzaprine Hydrochloride
- Product NDC
- 50090-3163
- 11-digit product format
- 500903163
- Labeler code
- 50090
- Product ID
- 50090-3163_315dfa64-8326-40b6-a5c8-5f1e8089d034
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-3163-0 | EA - Each | 50090-3163 | 38a08c75-c708-4c27-8b4d-54868d45d891 | 1 | 2019-05-02 |
| 50090-3163-1 | EA - Each | 50090-3163 | e0552ce7-cb6e-47cf-a99f-2a21256d33a9 | 1 | 2019-05-02 |
| 50090-3163-2 | EA - Each | 50090-3163 | ee93bdaf-8943-4a5c-a9f0-d58dfe1401e6 | 1 | 2019-05-02 |
| 50090-3163-3 | EA - Each | 50090-3163 | 1f8f28a6-9318-46b2-bc9c-d608e0afde29 | 1 | 2019-05-02 |
| 50090-3163-4 | EA - Each | 50090-3163 | 70f2525c-cce7-4c4f-8f3f-6ec2ba43f5ea | 1 | 2019-05-02 |
| 50090-3163-6 | EA - Each | 50090-3163 | 8336f55b-c645-40c7-9b2b-a5e8582d12bc | 1 | 2019-05-02 |
| 50090-3163-7 | EA - Each | 50090-3163 | 9decd9d3-30dc-425a-a8b3-8eea00fcb517 | 1 | 2019-05-02 |
| 50090-3163-8 | EA - Each | 50090-3163 | 8cbbd295-9c35-4fad-971f-73760179f777 | 1 | 2019-05-02 |
| 50090-3163-9 | EA - Each | 50090-3163 | 3250fd28-9739-4a39-975d-0e7912cd10e4 | 1 | 2019-05-02 |