Cyclobenzaprine hydrochloride
- Product NDC
- 55700-926
- 11-digit product format
- 557000926
- Labeler code
- 55700
- Product ID
- 55700-926_cd8640da-e890-44aa-a925-41aa29025462
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA213324
- Marketing category
- ANDA
- Marketing start
- 2021-10-05
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-926 | CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED [QUALITY CARE PRODUCTS, LLC] | 9 | Legacy NDC | 20241220_19a54d55-a79a-48c0-89d0-dedd0dcf9f45.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-926-01 | 55700092601 | 120 TABLET, FILM COATED in 1 BOTTLE (55700-926-01) | 2021-10-05 | 0000-00-00 | No | No | Current |
| 55700-926-18 | 55700092618 | 180 TABLET, FILM COATED in 1 BOTTLE (55700-926-18) | 2021-10-05 | 0000-00-00 | No | No | Current |
| 55700-926-30 | 55700092630 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-926-30) | 2021-10-05 | 0000-00-00 | No | No | Current |
| 55700-926-60 | 55700092660 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-926-60) | 2021-10-05 | 0000-00-00 | No | No | Current |
| 55700-926-90 | 55700092690 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-926-90) | 2021-10-05 | 0000-00-00 | No | No | Current |