NDC 68071-3462 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3462
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- cyclobenzaprine hydrochloride
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- May 31, 2017
- 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 |
|---|---|---|
| 68071-3462-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3462-2) | Jul 19, 2023 |
| 68071-3462-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3462-3) | Jul 31, 2023 |
| 68071-3462-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68071-3462-5) | Jul 19, 2023 |
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