NDC 70518-4692 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC70518-4692
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA218936
- Marketed since
- July 7, 2026
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4692-0 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-4692-0) | Jul 7, 2026 |
| 70518-4692-1 | 12 TABLET in 1 BOTTLE, PLASTIC (70518-4692-1) | Sep 2, 2026 |
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