NDC 85509-1035 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 15 mg/1 · Capsule, Extended Release · Oral
Product NDC85509-1035
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- PHOENIX RX LLC
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA091281
- Marketed since
- March 1, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 15 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 85509-1035-3 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (85509-1035-3) | Jan 19, 2026 |
| 85509-1035-6 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (85509-1035-6) | Jan 19, 2026 |
| 85509-1035-9 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (85509-1035-9) | Jan 19, 2026 |
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