Cyclobenzaprine Hydrochloride
- Product NDC
- 70518-0082
- 11-digit product format
- 705180082
- Labeler code
- 70518
- Product ID
- 70518-0082_e660509e-1f22-cede-e053-2995a90a42f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclobenzaprine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090478
- Marketing category
- ANDA
- Marketing start
- 2016-12-23
- Marketing end
- 0000-00-00
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 70518-0082-1 | 70518008201 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0082-1) | 2017-01-11 | 0000-00-00 | No | No | Current |
| 70518-0082-2 | 70518008202 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0082-2) | 2017-04-03 | 0000-00-00 | No | No | Current |
| 70518-0082-3 | 70518008203 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0082-3) | 2017-04-19 | 0000-00-00 | No | No | Current |
| 70518-0082-4 | 70518008204 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0082-4) | 2017-05-05 | 0000-00-00 | No | No | Current |
| 70518-0082-5 | 70518008205 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0082-5) | 2017-05-12 | 0000-00-00 | No | No | Current |
| 70518-0082-6 | 70518008206 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0082-6) | 2017-08-09 | 0000-00-00 | No | No | Current |