Cyclobenzaprine Hydrochloride
- Product NDC
- 70518-0191
- 11-digit product format
- 705180191
- Labeler code
- 70518
- Product ID
- 70518-0191_e6fff69b-1c12-dc53-e053-2a95a90a4345
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078048
- Marketing category
- ANDA
- Marketing start
- 2017-02-02
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0191-0 | 70518019100 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0191-0) | 2017-02-02 | 0000-00-00 | No | No | Current |
| 70518-0191-1 | 70518019101 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0191-1) | 2017-09-05 | 0000-00-00 | No | No | Current |
| 70518-0191-2 | 70518019102 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0191-2) | 2018-11-05 | 0000-00-00 | No | No | Current |
| 70518-0191-3 | 70518019103 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0191-3) | 2021-04-20 | 0000-00-00 | No | No | Current |