Tramadol Hydrochloride 72189-0311
Product NDC
72189-0311- Manufacturer
- Directrx
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- January 12, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA208708
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(9)
12 TABLET, COATED in 1 BOTTLE (72189-311-12)
20 TABLET, COATED in 1 BOTTLE (72189-311-20)
30 TABLET, COATED in 1 BOTTLE (72189-311-30)
40 TABLET, COATED in 1 BOTTLE (72189-311-40)
60 TABLET, COATED in 1 BOTTLE (72189-311-60)
120 TABLET, COATED in 1 BOTTLE (72189-311-72)
180 TABLET, COATED in 1 BOTTLE (72189-311-82)
240 TABLET, COATED in 1 BOTTLE (72189-311-84)
90 TABLET, COATED in 1 BOTTLE (72189-311-90)