NDC 69306-872 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC69306-872
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Doc Rx
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077563
- Marketed since
- July 31, 2025
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 69306-872-03 | 30 TABLET, FILM COATED in 1 BOTTLE (69306-872-03) | Oct 31, 2025 |
| 69306-872-06 | 60 TABLET, FILM COATED in 1 BOTTLE (69306-872-06) | Oct 31, 2025 |
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