NDC 68788-8474 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8474
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- July 1, 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8474-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-8474-2) | Jul 1, 2023 |
| 68788-8474-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8474-3) | Jul 1, 2023 |
| 68788-8474-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-8474-5) | Jul 1, 2023 |
| 68788-8474-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8474-6) | Jul 1, 2023 |
| 68788-8474-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8474-9) | Jul 1, 2023 |
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