NDC 68071-2659 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-2659
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- NuCare Pharmaceuticals,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
- Cyclobenzaprine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68071-2659-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-2659-3) | Mar 28, 2022 |
| 68071-2659-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68071-2659-5) | Mar 28, 2022 |
| 68071-2659-6 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-2659-6) | Oct 14, 2024 |
| 68071-2659-7 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-2659-7) | Dec 2, 2024 |
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