Tramadol Hydrochloride 68071-4119
Product NDC
68071-4119- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- November 15, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA076003
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(8)
120 TABLET, COATED in 1 BOTTLE (68071-4119-1)
30 TABLET, COATED in 1 BOTTLE (68071-4119-3)
40 TABLET, COATED in 1 BOTTLE (68071-4119-4)
15 TABLET, COATED in 1 BOTTLE (68071-4119-5)
60 TABLET, COATED in 1 BOTTLE (68071-4119-6)
84 TABLET, COATED in 1 BOTTLE (68071-4119-7)
180 TABLET, COATED in 1 BOTTLE (68071-4119-8)
90 TABLET, COATED in 1 BOTTLE (68071-4119-9)