NDC 71335-1099 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1099
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, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1099-0 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1099-0) | Feb 22, 2019 |
| 71335-1099-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1099-1) | Feb 22, 2019 |
| 71335-1099-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1099-2) | Feb 22, 2019 |
| 71335-1099-3 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-1099-3) | Feb 22, 2019 |
| 71335-1099-4 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1099-4) | Feb 22, 2019 |
| 71335-1099-5 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1099-5) | Feb 22, 2019 |
| 71335-1099-6 | 40 TABLET, FILM COATED in 1 BOTTLE (71335-1099-6) | Feb 22, 2019 |
| 71335-1099-7 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1099-7) | Feb 22, 2019 |
| 71335-1099-8 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1099-8) | Feb 22, 2019 |
| 71335-1099-9 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1099-9) | Feb 22, 2019 |
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