NDC 68071-3150 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3150
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 (9)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3150-1 | 21 TABLET, FILM COATED in 1 BOTTLE (68071-3150-1) | Mar 7, 2017 |
| 68071-3150-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3150-2) | Mar 7, 2017 |
| 68071-3150-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3150-3) | Mar 7, 2017 |
| 68071-3150-4 | 84 TABLET, FILM COATED in 1 BOTTLE (68071-3150-4) | Mar 16, 2017 |
| 68071-3150-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68071-3150-5) | Mar 7, 2017 |
| 68071-3150-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3150-6) | Mar 7, 2017 |
| 68071-3150-7 | 7 TABLET, FILM COATED in 1 BOTTLE (68071-3150-7) | Mar 7, 2017 |
| 68071-3150-8 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-3150-8) | Mar 7, 2017 |
| 68071-3150-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3150-9) | Mar 7, 2017 |
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