NDC 71335-2666 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71335-2666
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA218936
- Marketed since
- February 19, 2025
- 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 (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2666-0 | 40 TABLET in 1 BOTTLE (71335-2666-0) | Jul 14, 2025 |
| 71335-2666-1 | 14 TABLET in 1 BOTTLE (71335-2666-1) | Jul 14, 2025 |
| 71335-2666-2 | 84 TABLET in 1 BOTTLE (71335-2666-2) | Jul 14, 2025 |
| 71335-2666-3 | 30 TABLET in 1 BOTTLE (71335-2666-3) | Jul 14, 2025 |
| 71335-2666-4 | 20 TABLET in 1 BOTTLE (71335-2666-4) | Jul 14, 2025 |
| 71335-2666-5 | 15 TABLET in 1 BOTTLE (71335-2666-5) | Jul 14, 2025 |
| 71335-2666-6 | 60 TABLET in 1 BOTTLE (71335-2666-6) | Jul 14, 2025 |
| 71335-2666-7 | 90 TABLET in 1 BOTTLE (71335-2666-7) | Jul 14, 2025 |
| 71335-2666-8 | 56 TABLET in 1 BOTTLE (71335-2666-8) | Jul 14, 2025 |
| 71335-2666-9 | 120 TABLET in 1 BOTTLE (71335-2666-9) | Jul 14, 2025 |
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