NDC 71335-2156 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2156
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
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2156-0 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2156-0) | Aug 22, 2022 |
| 71335-2156-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2156-1) | Aug 22, 2022 |
| 71335-2156-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2156-2) | Aug 22, 2022 |
| 71335-2156-3 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-2156-3) | Aug 22, 2022 |
| 71335-2156-4 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2156-4) | Aug 22, 2022 |
| 71335-2156-5 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-2156-5) | Aug 22, 2022 |
| 71335-2156-6 | 40 TABLET, FILM COATED in 1 BOTTLE (71335-2156-6) | Aug 22, 2022 |
| 71335-2156-7 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2156-7) | Aug 22, 2022 |
| 71335-2156-8 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2156-8) | Aug 22, 2022 |
| 71335-2156-9 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2156-9) | Aug 22, 2022 |
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