NDC 70518-4751 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4751
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- September 13, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 7.5 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4751-0 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4751-0) | Sep 13, 2026 |
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