NDC 65862-191 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-191
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078643
- Marketed since
- September 26, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 65862-191-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-191-01) | Sep 26, 2008 |
| 65862-191-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-191-05) | Sep 26, 2008 |
| 65862-191-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-191-99) | Sep 26, 2008 |
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