NDC 70518-4265 – Cyclobenzaprine hydrochloride
Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4265
Product details
- Brand name
- Cyclobenzaprine hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213324
- Marketed since
- January 24, 2025
- 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 |
|---|---|---|
| 70518-4265-0 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4265-0) | Jan 24, 2025 |
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