NDC 70518-3474 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3474
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
- August 9, 2022
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3474-2 | 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-2) | Aug 13, 2022 |
| 70518-3474-4 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-4) | Aug 23, 2022 |
| 70518-3474-5 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-5) | Aug 23, 2022 |
| 70518-3474-7 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-7) | Sep 29, 2022 |
| 70518-3474-8 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-8) | Nov 9, 2022 |
| 70518-3474-9 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-9) | Dec 1, 2022 |
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