NDC 85509-1001 – Cyclobenzaprine HCL
Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC85509-1001
Product details
- Brand name
- Cyclobenzaprine HCL
- Generic name
- Cyclobenzaprine HCL
- Labeler
- PHOENIX RX LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078722
- Marketed since
- March 25, 2015
- 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 HCL →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 85509-1001-1 | 120 TABLET, FILM COATED in 1 BOTTLE (85509-1001-1) | Jul 21, 2025 |
| 85509-1001-3 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1001-3) | Jul 21, 2025 |
| 85509-1001-6 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1001-6) | Jul 21, 2025 |
| 85509-1001-9 | 90 TABLET, FILM COATED in 1 BOTTLE (85509-1001-9) | Jul 21, 2025 |
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