NDC 71335-2110 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2110
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078643
- Marketed since
- September 26, 2008
- 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 |
|---|---|---|
| 71335-2110-0 | 40 TABLET, FILM COATED in 1 BOTTLE (71335-2110-0) | Jun 20, 2022 |
| 71335-2110-1 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-2110-1) | Jun 20, 2022 |
| 71335-2110-2 | 84 TABLET, FILM COATED in 1 BOTTLE (71335-2110-2) | Jun 20, 2022 |
| 71335-2110-3 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2110-3) | Jun 20, 2022 |
| 71335-2110-4 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2110-4) | Jun 20, 2022 |
| 71335-2110-5 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-2110-5) | Jun 20, 2022 |
| 71335-2110-6 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2110-6) | Jun 20, 2022 |
| 71335-2110-7 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2110-7) | Jun 20, 2022 |
| 71335-2110-8 | 56 TABLET, FILM COATED in 1 BOTTLE (71335-2110-8) | Jun 20, 2022 |
| 71335-2110-9 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2110-9) | Jun 20, 2022 |
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