NDC 59746-735 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC59746-735
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077563
- Marketed since
- October 9, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 7.5 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 59746-735-01 | 100 TABLET, FILM COATED in 1 BOTTLE (59746-735-01) | Oct 9, 2017 |
| 59746-735-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (59746-735-10) | Oct 9, 2017 |
| 59746-735-30 | 30 TABLET, FILM COATED in 1 BOTTLE (59746-735-30) | Oct 9, 2017 |
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