NDC 71335-0096 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0096
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078722
- Marketed since
- March 25, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 7.5 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0096-0 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0096-0) | Mar 9, 2022 |
| 71335-0096-1 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0096-1) | Mar 20, 2018 |
| 71335-0096-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0096-2) | Mar 5, 2018 |
| 71335-0096-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0096-3) | Mar 20, 2018 |
| 71335-0096-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0096-4) | May 9, 2018 |
| 71335-0096-5 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0096-5) | Sep 27, 2019 |
| 71335-0096-6 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-0096-6) | Mar 9, 2022 |
| 71335-0096-7 | 9 TABLET, FILM COATED in 1 BOTTLE (71335-0096-7) | Sep 4, 2018 |
| 71335-0096-8 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0096-8) | Mar 9, 2022 |
| 71335-0096-9 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0096-9) | Apr 23, 2018 |
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