Cyclobenzaprine Hydrochloride
- Product NDC
- 55700-229
- 11-digit product format
- 557000229
- Labeler code
- 55700
- Product ID
- 55700-229_9a95a326-9bd0-491d-bac9-feea9f92bd99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077797
- Marketing category
- ANDA
- Marketing start
- 2007-02-28
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 5 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 |
|---|---|---|---|---|---|
| 55700-229-10 | EA - Each | 55700-229 | 39b90757-2ed9-4f92-98fa-cb22145e8153 | 1 | 2016-05-16 |
| 55700-229-12 | EA - Each | 55700-229 | e9454952-364a-4f81-921c-74309b4151e6 | 1 | 2016-05-16 |
| 55700-229-15 | EA - Each | 55700-229 | 7757eed7-c9d4-4edc-b273-ed951deab739 | 1 | 2016-05-16 |
| 55700-229-20 | EA - Each | 55700-229 | 2ff63da9-e80f-458e-88c0-ecec6dc9b7a0 | 1 | 2016-05-16 |
| 55700-229-21 | EA - Each | 55700-229 | e20ca287-b2b9-4fb7-82d1-97a688170d37 | 1 | 2016-05-16 |
| 55700-229-30 | EA - Each | 55700-229 | b3c198a9-bb2a-4f4a-8605-ce010e5770d5 | 1 | 2016-05-16 |
| 55700-229-60 | EA - Each | 55700-229 | 4a4a0321-cc47-4a5c-9294-163565183990 | 1 | 2016-05-16 |
| 55700-229-90 | EA - Each | 55700-229 | 4e426c8e-b1bd-405d-83d7-4e5130a291df | 1 | 2016-05-16 |