NDC 70518-3764 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3764
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078643
- Marketed since
- June 13, 2023
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 70518-3764-0 | 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-0) | Jun 13, 2023 |
| 70518-3764-1 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-1) | Mar 5, 2024 |
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