NDC 80425-0019 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC80425-0019
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077797
- Marketed since
- March 30, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0019-1 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0019-1) | Mar 30, 2017 |
| 80425-0019-2 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0019-2) | Mar 30, 2017 |
| 80425-0019-3 | 90 TABLET, FILM COATED in 1 BOTTLE (80425-0019-3) | Mar 30, 2017 |
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