NDC 42708-172 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC42708-172
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- QPharma Inc
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 42708-172-20 sample | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-172-20) | May 19, 2023 |
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