NDC 70518-3814 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3814
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- August 1, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3814-0 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-0) | Aug 1, 2023 |
| 70518-3814-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-1) | Aug 2, 2023 |
| 70518-3814-2 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-2) | Aug 18, 2023 |
| 70518-3814-3 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-3) | Oct 7, 2023 |
| 70518-3814-5 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-5) | Dec 23, 2023 |
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