Cyclobenzaprine Hydrochloride
- Product NDC
- 50090-2644
- 11-digit product format
- 500902644
- Labeler code
- 50090
- Product ID
- 50090-2644_8b8b7e67-acfa-4582-b061-010b70b8ed42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078218
- Marketing category
- ANDA
- Marketing start
- 2010-02-18
- 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 |
|---|---|---|---|---|---|
| 50090-2644-0 | EA - Each | 50090-2644 | 91bee402-aeae-47d1-a198-1608da360816 | 1 | 2019-04-11 |
| 50090-2644-1 | EA - Each | 50090-2644 | 782a1fa8-3e68-45cd-8a1c-4a79cc9b0a6d | 1 | 2019-04-11 |
| 50090-2644-2 | EA - Each | 50090-2644 | 80a34244-b82e-4b46-adc9-79442bc0874f | 1 | 2018-11-06 |
| 50090-2644-3 | EA - Each | 50090-2644 | 90ab430f-14f6-4143-b95a-a1e791c97063 | 1 | 2018-11-06 |
| 50090-2644-4 | EA - Each | 50090-2644 | 106eb979-6529-45fb-b4e5-0af84c93344a | 1 | 2018-11-06 |
| 50090-2644-6 | EA - Each | 50090-2644 | 2b4543bb-984a-402a-8317-40bc4a81923f | 1 | 2019-04-11 |
| 50090-2644-8 | EA - Each | 50090-2644 | 004b963c-7581-4e03-96b2-b056dce157b1 | 1 | 2019-04-11 |
| 50090-2644-9 | EA - Each | 50090-2644 | e2bea752-dd40-4778-840b-7225a531c453 | 1 | 2019-04-11 |