NDC 68071-3154 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3154
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090478
- Marketed since
- July 22, 2016
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3154-1 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-3154-1) | May 17, 2017 |
| 68071-3154-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3154-3) | May 17, 2017 |
| 68071-3154-6 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-3154-6) | May 17, 2017 |
| 68071-3154-7 | 7 TABLET, FILM COATED in 1 BOTTLE (68071-3154-7) | May 17, 2017 |
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