CYCLOBENZAPRINE HYROCHLORIDE
- Product NDC
- 63629-4664
- 11-digit product format
- 636294664
- Labeler code
- 63629
- Product ID
- 63629-4664_5268b5ff-4092-4806-9957-5031002a8fba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYCLOBENZAPRINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078722
- Marketing category
- ANDA
- Marketing start
- 2011-08-29
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-4664-1 | EA - Each | 63629-4664 | 49ebbf15-cbd9-477e-9af8-818a338abb8b | 1 | 2013-02-13 |
| 63629-4664-2 | EA - Each | 63629-4664 | 5a88e154-5624-4653-b4a8-9ef5b4618024 | 1 | 2013-02-13 |
| 63629-4664-3 | EA - Each | 63629-4664 | 13708cb7-5d4d-4649-b547-bc741d6c2a1c | 1 | 2013-02-13 |
| 63629-4664-4 | EA - Each | 63629-4664 | 2b05b2bc-bf94-4299-994a-0efc9a48487c | 1 | 2013-02-13 |
| 63629-4664-5 | EA - Each | 63629-4664 | d3222949-89bd-4181-9a55-37d4c6b157e0 | 1 | 2015-10-02 |
| 63629-4664-6 | EA - Each | 63629-4664 | ce8e9b96-9800-456b-a9a6-fb0adcdb58b2 | 1 | 2015-10-02 |
| 63629-4664-7 | EA - Each | 63629-4664 | 07202414-3dd6-4449-a92f-d5fd00af665c | 1 | 2015-10-02 |