NDC 51655-592 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-592
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- January 3, 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 51655-592-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-20) | Jan 31, 2023 |
| 51655-592-25 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-25) | May 2, 2023 |
| 51655-592-26 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-26) | Feb 7, 2023 |
| 51655-592-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-52) | Jan 3, 2023 |
| 51655-592-53 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-53) | Jan 3, 2023 |
| 51655-592-54 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-54) | Jan 3, 2023 |
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