Tramadol Hydrochloride 72189-0154
Product NDC
72189-0154- Manufacturer
- Direct Rx
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- November 10, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA200503
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 (72189-154-30)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-154-60)