Tramadol Hydrochloride 68071-3655
Product NDC
68071-3655- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- March 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA202075
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(3)
12 TABLET in 1 PACKAGE (68071-3655-2)
4 TABLET in 1 PACKAGE (68071-3655-4)
6 TABLET in 1 PACKAGE (68071-3655-6)