NDC 70518-3251 – Cyclobenzaprine hydrochloride
Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3251
Product details
- Brand name
- Cyclobenzaprine hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213324
- Marketed since
- October 20, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3251-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-1) | Nov 16, 2021 |
| 70518-3251-2 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3251-2) | Nov 23, 2021 |
| 70518-3251-6 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-6) | Jun 9, 2025 |
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