NDC 85509-1415 – Cyclobenzaprine hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC85509-1415
Product details
- Brand name
- Cyclobenzaprine hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- PHOENIX RX LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213324
- Marketed since
- July 6, 2020
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 85509-1415-3 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1415-3) | Nov 14, 2025 |
| 85509-1415-6 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1415-6) | Nov 14, 2025 |
| 85509-1415-9 | 90 TABLET, FILM COATED in 1 BOTTLE (85509-1415-9) | Nov 14, 2025 |
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