NDC 68788-9967 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-9967
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078722
- Marketed since
- May 1, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 7.5 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 68788-9967-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-9967-1) | May 1, 2015 |
| 68788-9967-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-9967-2) | May 1, 2015 |
| 68788-9967-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-9967-3) | May 1, 2015 |
| 68788-9967-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-9967-6) | May 1, 2015 |
| 68788-9967-7 | 8 TABLET, FILM COATED in 1 BOTTLE (68788-9967-7) | Aug 14, 2019 |
| 68788-9967-8 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-9967-8) | May 1, 2015 |
| 68788-9967-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-9967-9) | May 1, 2015 |
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