NDC 71335-2686 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2686
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- May 31, 2017
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 71335-2686-1 | 5 TABLET, FILM COATED in 1 BOTTLE (71335-2686-1) | Sep 18, 2025 |
| 71335-2686-2 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2686-2) | Sep 18, 2025 |
| 71335-2686-3 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-2686-3) | Sep 18, 2025 |
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