CYCLOBENZAPRINE HYDROCHLORIDE
- Product NDC
- 63187-123
- 11-digit product format
- 631870123
- Labeler code
- 63187
- Product ID
- 63187-123_d88c45a4-7478-497d-93e1-15629181f650
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYCLOBENZAPRINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63187-123-60 | 2019-12-10 | C162847 | 48780-1 | 9855e2a2-34f2-60a7-e053-dbdaa90a05bd | d88c45a4-7478-497d-93e1-15629181f650 |
| 63187-123-72 | 2019-12-10 | C162847 | 48780-1 | 9855e2a2-34f2-60a7-e053-dbdaa90a05bd | d88c45a4-7478-497d-93e1-15629181f650 |
| 63187-123-90 | 2019-12-10 | C162847 | 48780-1 | 9855e2a2-34f2-60a7-e053-dbdaa90a05bd | d88c45a4-7478-497d-93e1-15629181f650 |
| 63187-123-60 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-34f2-60a7-e053-dbdaa90a05bd | d88c45a4-7478-497d-93e1-15629181f650 |
| 63187-123-72 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-34f2-60a7-e053-dbdaa90a05bd | d88c45a4-7478-497d-93e1-15629181f650 |
| 63187-123-90 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-34f2-60a7-e053-dbdaa90a05bd | d88c45a4-7478-497d-93e1-15629181f650 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63187-123-60 | EA - Each | 63187-123 | 2e561ecb-7e2f-48c0-868a-f932798abb6a | 1 | 2015-03-03 |