NDC 68788-8167 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8167
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078643
- Marketed since
- April 8, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8167-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-8167-2) | Apr 8, 2022 |
| 68788-8167-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8167-3) | Apr 8, 2022 |
| 68788-8167-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-8167-5) | Apr 8, 2022 |
| 68788-8167-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8167-6) | Apr 8, 2022 |
| 68788-8167-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8167-9) | Apr 8, 2022 |
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