Tramadol Hydrochloride 61919-0893
Product NDC
61919-0893- Manufacturer
- Direct Rx
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- January 1, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA201384
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 200 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-30)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-60)