NDC 51655-973 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-973
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090478
- Marketed since
- May 4, 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 |
|---|---|---|
| 51655-973-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-20) | Oct 17, 2022 |
| 51655-973-25 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-25) | Sep 6, 2022 |
| 51655-973-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-52) | Oct 7, 2022 |
| 51655-973-53 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-53) | Jul 27, 2022 |
| 51655-973-54 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-54) | Aug 24, 2022 |
| 51655-973-87 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-87) | May 4, 2022 |
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